HOO
1994-06-06
Perimeter, Ac-Powered
FDA product code HOO · 6 cleared devices
Class 1
Ophthalmic
- Regulation
- 21 CFR 886.1605
- Review panel
- OP
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1983-09-29 – 1994-06-06
HOO
1993-06-21
MARCO PROJECTION PERIMETER
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HOO
1987-11-02
RICHMOND VISUAL FIELD SCREENER
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HOO
1986-12-15
HENSON - HAMBLIN CFS 2000 CENTRAL FIELD SCREEN
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HOO
1986-02-27
DIGILAB CAMBRIDGE PERIMETER
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HOO
1983-09-29
AUTOMATIC TANGENT SCREEN 50
View details →No matching devices.
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