HGF
1995-01-26
Source, Abortion Unit, Vacuum
FDA product code HGF · 4 cleared devices
Class 2
Obstetrics/Gynecology
- Regulation
- 21 CFR 884.5070
- Review panel
- OB
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1989-03-24 – 1995-01-26
HGF
1991-02-11
BIOVISION ENDOCULAR PROBE
View details →
HGF
1990-12-14
MODEL GLASE 210 HOLMIUM LASER SYSTEM
View details →
HGF
1989-03-24
O-020 LASER INDIRECT OPHTHALMOSCOPE
View details →No matching devices.
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