Medical Device Manufacturer · US , Irvine , CA

Biovision AG - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2002
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
K042083 · HNO
Ophthalmic · 105d
Cleared Mar 11, 2002
VISTITOME 20-10 MICROKERATOME
K014000 · HNO
Ophthalmic · 97d
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