Medical Device Manufacturer · US , Lafayette , IN

Lafayette Pharmacal, Inc. - FDA 510(k) Cleared Devices

4 submissions · 3 cleared · Since 1986

Total

Cleared

Denied

Lafayette Pharmacal, Inc. has 3 FDA 510(k) cleared medical devices. Based in Lafayette, US.

Historical record: 3 cleared submissions from 1986 to 1993. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) Regulatory Record - Lafayette Pharmacal, Inc.

4 devices

1-4 of 4