GRO
1985-07-08
Antisera, Fluorescent, All Types, Hemophilus Spp.
FDA product code GRO · 4 cleared devices
Class 2
Microbiology
- Regulation
- 21 CFR 866.3300
- Review panel
- MI
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1980-04-04 – 1985-07-08
GRO
1984-01-03
LEGIONELLA DIFFERENTIATION DISK
View details →
GRO
1980-11-12
PHADEBACT HAEMOPHILUS TEST
View details →
GRO
1980-04-04
BACTOGEN-H. INFLUENZAE TYPE B
View details →No matching devices.