Medical Device Manufacturer · DE , Erlangen

Wavelight AG - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2007

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Wavelight AG Ophthalmic ✕

1 devices

1-1 of 1

Cleared Jul 20, 2007

ALLEGRO OCULYZER

Ophthalmic · 81d