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Reagent/Device, Inoculum Calibration

FDA product code LIE · 7 cleared devices

Class 2 Microbiology
Regulation
21 CFR 866.1640
Review panel
MI
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1982-03-15 – 2023-04-05
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