KEL
1989-01-10
Adhesive, Albumin-Based
FDA product code KEL · 2 cleared devices
Class 1
Pathology
- Regulation
- 21 CFR 864.4010
- Review panel
- PA
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- Yes
- Clearance span
- 1988-04-18 – 1989-01-10
KEL
1988-04-18
HISTOGRIP & HISTOGRIP GOLD CONCENTRATE/PREDILUTED
View details →No matching devices.
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