Medical Device Manufacturer · US , Washington , DC

Lase, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1987

3

Total

3

Cleared

0

Denied

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

2 devices

1-2 of 2

Cleared Mar 21, 1988

LASE EVACUATOR/ASPIRATOR

General & Plastic Surgery · 160d

Cleared Jun 01, 1987

General & Plastic Surgery · 59d