HJA
1990-06-27
Photokeratoscope
FDA product code HJA · 5 cleared devices
Class 1
Ophthalmic
- Regulation
- 21 CFR 886.1350
- Review panel
- OP
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1978-10-17 – 1990-06-27
HJA
1989-09-11
VKG 2000 VIDEO KERATOMETER
View details →
HJA
1984-08-07
AMERICAN MEDICAL OPTICS PHOTOKERATO
View details →
HJA
1983-03-09
DORC CONTACT/PHOTO DERATOSCOPE
View details →
HJA
1978-10-17
TERRY KERATOMETER
View details →No matching devices.
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