Medical Device Manufacturer · US , MA

Louis M. Gerson Co., Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1980

Total

Cleared

Denied

Louis M. Gerson Co., Inc. has 8 FDA 510(k) cleared medical devices. Based in US.

Historical record: 8 cleared submissions from 1980 to 2006. Primary specialty: General Hospital.

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

Louis M. Gerson Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Louis M. Gerson Co., Inc.

8 devices

1-8 of 8