IFB
1985-06-10
Cytocentrifuge
FDA product code IFB · 3 cleared devices
Class 1
Pathology
- Regulation
- 21 CFR 864.3300
- Review panel
- PA
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1979-11-30 – 1985-06-10
IFB
1981-04-23
CYTOBUCKET MODEL 1024
View details →
IFB
1979-11-30
LEIF CENTRIFUGAL CYTOLOGY BUCKET
View details →No matching devices.
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