Medical Device Manufacturer · US , East Rockaway , NY

Laivan Corp. - FDA 510(k) Cleared Devices

6 submissions · 2 cleared · Since 1988

6

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Laivan Corp. General & Plastic Surgery ✕

5 devices

1-5 of 5

Cleared Apr 17, 1989

MODIFIED LABELING FOR POLYDERM WBC(TM)

General & Plastic Surgery · 54d

Cleared Mar 29, 1989

General & Plastic Surgery · 100d

Cleared Apr 13, 1988

POLYDERM A+B(TM)

General & Plastic Surgery · 91d

Cleared Mar 17, 1988

POLYDERM PEC(TM), POROUS ELASTIC COVER

General & Plastic Surgery · 9d

Cleared Mar 11, 1988

POLYDERM WBC (TM), WATERPROOF BREATHABLE COVER

General & Plastic Surgery · 56d