HLW
1990-02-09
Preamplifier, Battery-Powered, Ophthalmic
FDA product code HLW · 3 cleared devices
Class 2
Ophthalmic
- Regulation
- 21 CFR 886.1640
- Review panel
- OP
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1986-02-18 – 1990-02-09
HLW
1990-02-09
MONOPOLAR NEEDLE ELECTRODE
View details →
HLW
1986-02-18
MONOPOLAR INJECTION NEEDLE ELECTRODE
View details →No matching devices.
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