Medical Device Manufacturer · US , Santa Barbara , CA

Laserguide - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1987

Total

Cleared

Denied

Laserguide has 5 FDA 510(k) cleared medical devices. Based in Santa Barbara, US.

Historical record: 5 cleared submissions from 1987 to 1988. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Laserguide Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Laserguide

5 devices

1-5 of 5