Medical Device Manufacturer · US , Palm Harbor , FL

L H M Ent., Inc. - FDA 510(k) Cleared Devices

6 submissions · 4 cleared · Since 1988

Total

Cleared

Denied

L H M Ent., Inc. has 4 FDA 510(k) cleared medical devices. Based in Palm Harbor, US.

Historical record: 4 cleared submissions from 1988 to 1990.

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

L H M Ent., 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 - L H M Ent., Inc.

6 devices

1-6 of 6