Medical Device Manufacturer · US , Ft Lauderdale , FL

Neogen Technologies, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2003

Recent clearances: NEOGEN ONE, CLOSED WOUND DRAIN SYSTEM, PART NUMBER: NG9900

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Neogen Technologies, Inc. General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Aug 21, 2003

NEOGEN ONE, CLOSED WOUND DRAIN SYSTEM, PART NUMBER: NG9900

General & Plastic Surgery · 27d