Medical Device Manufacturer · US , Washington , DC

Carl Zeiss Jena GmbH - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2001

Recent clearances: FF450 PLUS FUNDUS CAMERA AND VISUPAC DIGITAL IMAGE ARCHIVING SYSTEM, OR FF450 PLUS VISUPAC SYSTEM

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Carl Zeiss Jena GmbH Ophthalmic ✕

1 devices

1-1 of 1

Cleared Sep 26, 2001

FF450 PLUS FUNDUS CAMERA AND VISUPAC DIGITAL IMAGE ARCHIVING SYSTEM, OR FF450...

Ophthalmic · 103d