Instrument, Vitreous Aspiration And Cutting, Battery-Powered
FDA product code HKP · 16 cleared devices
Class 2
Ophthalmic
- Regulation
- 21 CFR 886.4150
- Review panel
- OP
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1976-10-05 – 1997-03-19
HKP
1997-03-19
HKP
1995-05-05
THE GRIESHABER AXIAL CUTTER
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HKP
1995-04-10
UNIVIT PROBE
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HKP
1990-04-04
VISITEC VITRECTOMY UNIT
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HKP
1989-04-17
MENTOR ANTERIOR SEGMENT VITRECTOR
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HKP
1983-08-01
CAVITRON/KELMAN PHACO-EMULSIFIER ASPIRA
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HKP
1982-10-06
KEATES I/A SYSTEM FRIGITRONICS 4000
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HKP
1981-12-31
EMERGENCY POWER PAC (EMPAC)
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HKP
1981-03-17
X-VEE
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HKP
1980-07-21
EYE-VAC
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HKP
1979-10-30
OCUTOME MODEL 8000
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HKP
1979-09-04
VITREOUS SUCTION/CUTTER
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HKP
1979-08-28
STAT
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HKP
1978-11-03
CLINITEX VIS-X ASPIRATING ACCESSORY
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HKP
1977-01-05
VITEROUS SUCTION CUTTER
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HKP
1976-10-05
VISC X-VITREOUS ASPIRATING & CUT. INSTR
View details →No matching devices.
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