FDA Home Page | CDRH Home Page | Search | CDRH A-Z Index | Contact CDRH

Radiological Devices Panel Meeting Summary for December 10, 2002

The Radiological Devices Panel met on December 10, 2002, to discuss and vote on an original premarket approval (PMA) application, P010035 from Computerized Thermal Imaging, Inc. for their BCS 2100. The device produces a thermal image of the breast in women recommended for biopsy, and from this image the computer yields a result indicating whether or not the biopsy is still recommended.

Following a discussion of the issues associated with this PMA, the Panel's recommendation was "not approvable" by a 4 to 3 vote.

The consensus was that new trial data are needed because, from the clinical data presented, there were too many questions that remained unanswered to conclude that the device is safe and effective. The minority questioned whether a reanalysis of the existing data and/or a post-market study might help answer the outstanding questions.

Contact: Robert J. Doyle, Executive Secretary
(301) 594-1212, x124

Transcripts may be purchased from (written requests only):
Neak R, Gross & Company
1323 Rhode Island Avenue, N.W.
Washington, DC 20005
(202) 234-4433 (voice)
or
Food and Drug Administration
Freedom of Information Staff (FOI)
5600 Fishers Lane, HFI-35
Rockville, MD 20852
(301) 827-6500 (voice)/(301) 443-1726 (fax)

Under normal circumstances, panel summary minutes are available 60-90 days post meeting. Summaries are also available on the CDRH website: http://www.fda.gov/cdrh/panel/

Back to CDRH Advisory Committee Database

Updated 12/26/02

CDRH Home Page | CDRH A-Z Index | Contact CDRH | Accessibility | Disclaimer
FDA Home Page | Search FDA Site | FDA A-Z Index | Contact FDA | HHS Home Page

Center for Devices and Radiological Health / CDRH