Federal Register: November 14, 2000 (Volume 65, Number 220)
DOCID: FR Doc 00-29110
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
Docket ID: [Docket No. 00D-1587]
ACTION: Reports and guidance documents; availability, etc.:
DOCUMENT ACTION: Notice.
Medical Devices Draft Guidance on Guidance for Prescription Use Drugs of Abuse Assays Premarket Notifications; Availability
DATES: Submit written comments on the draft guidance by February 12, 2001.
The Food and Drug Administration (FDA) is announcing the availability of the draft guidance entitled ``Guidance for Prescription Use Drugs of Abuse Assays Premarket Notifications.'' FDA is issuing this guidance to express the general principles FDA applies in evaluating premarket notifications (510(k)s) for prescription use drugs of abuse assays. The principles described in this draft guidance document apply only to in vitro diagnostic (IVD) submissions for 510(k) clearance for these devices. This draft guidance is neither final nor in effect at this time.
Prescription use drugs of abuse assays premarket notifications,
This draft guidance recommends data and labeling that manufacturers should submit in support of substantial equivalence for prescription use drugs of abuse assays. The recommendations and general principles in this draft guidance are provided to assist manufacturers in the preparation of premarket notifications (510(k)s) for these devices. This document will supersede the document, ``Review Criteria for Assessment of In Vitro Diagnostic Devices for Drugs of Abuse Assays Using Various Methodologies,'' August 31, 1995. This draft guidance explains the types of studies to conduct and how to present the study data in greater detail than the document it is replacing.
II. Significance of Guidance
This draft guidance represents the agency's current thinking regarding data and labeling for prescription use drugs of abuse device submissions for 510(k) clearance. It does not create or confer any rights for or on any person and does not operate to bind FDA or the public. An alternative approach may be used if such approach satisfies the applicable statute, regulations, or both.
The agency has adopted good guidance practices (GGP's) and published the final rule, which set forth the agency's regulations for the development, issuance, and use of guidance documents (65 FR 56468, September 19, 2000). This guidance document is issued as a Level 1 draft guidance consistent with the GGP's.
III. Electronic Access
In order to receive the draft guidance entitled ``Guidance for Prescription Use Drugs of Abuse Assays Premarket Notifications'' via your fax machine, call the CDRH FactsOnDemand system at 8008990381 or 3018270111 from a touchtone telephone. Press 1 to enter the system. At the second voice prompt press 1 to order a document. Enter the document number (152) followed by the pound sign (#). Follow the remaining voice prompts to complete your request.
Persons interested in obtaining a copy of the guidance may also do so using the Internet. The Center for Devices and Radiological Health (CDRH) maintains an entry on the Internet for easy access to information including text, graphics, and files that may be downloaded to a personal computer with access to the Internet. Updated on a regular basis, the CDRH home page includes the civil money penalty guidance documents package, device safety alerts, Federal Register reprints, information on premarket submissions (including lists of approved applications and manufacturers' addresses), small manufacturers' assistance, information on video conferencing and electronic submissions, mammography matters, and other deviceoriented information. The CDRH home page may be accessed at http://www.fda.gov/ cdrh. ``Guidance for Prescription Use Drugs of Abuse Assays Premarket Notifications'' will be available at http://www.fda.gov/cdrh/ode/ guidance/152.pdf.
Interested persons may submit to Dockets Management Branch (address above) written comments regarding this draft guidance by February 12, 2001. Two copies of any comments are to be submitted, except individuals may submit one copy. Comments are to be identified with the docket number found in brackets in the heading of this document. The draft guidance and received comments may be seen in the Dockets Management Branch between 9 a.m. and 4 p.m., Monday through Friday.
Dated: November 2, 2000.
Linda S. Kahan,
Deputy Director for Regulations Policy, Center for Devices and Radiological Health.
[FR Doc. 0029110 Filed 11800; 4:21 pm] BILLING CODE 416001F
FOR FURTHER INFORMATION CONTACT
Jean M. Cooper, Center for Devices and Radiological Health (HFZ440), Food and Drug Administration, 9200 Corporate Blvd., Rockville, MD 20850, 3015941243.