Medical Device Manufacturer · US , Pasadena , CA

Femtek, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1996
1
Total
1
Cleared
0
Denied

Femtek, Inc. has 1 FDA 510(k) cleared medical devices. Based in Pasadena, US.

Historical record: 1 cleared submissions from 1996 to 1996. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Femtek, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Femtek, Inc.

1 devices
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