Medical Device Manufacturer · US , Irvine , CA

Biovision AG - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2002

Recent clearances: MODIFICATION TO VISITOME 20-10 MICROKERATOME, VISTITOME 20-10 MICROKERATOME

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

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

2 devices

1-2 of 2

Cleared Nov 16, 2004

MODIFICATION TO VISITOME 20-10 MICROKERATOME

Ophthalmic · 105d

Cleared Mar 11, 2002

VISTITOME 20-10 MICROKERATOME

Ophthalmic · 97d