Retinoscope, Battery-Powered
FDA product code HKM · 7 cleared devices
Class 1
Ophthalmic
- Regulation
- 21 CFR 886.1780
- Review panel
- OP
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- Yes
- Clearance span
- 1984-07-12 – 1997-01-09
HKM
1997-01-09
HKM
1995-03-28
STREAK RETINOSCOPE RX-RP
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HKM
1995-03-28
STREAK RETINOSCOPE RX-RC
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HKM
1995-03-28
SPOT RETINOSCOPE RX-3SP
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HKM
1995-03-28
STREAK RETINOSCOPE RX-3A
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HKM
1995-03-28
STREAK RETINOSCOPE RX-3
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HKM
1984-07-12
GENERATED RETINAL REFLEX IMAGERY SYS
View details →No matching devices.
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