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Antisera, Fluorescent, Chlamydia Spp.

FDA product code LKI · 6 cleared devices

Class 1 Microbiology
Regulation
21 CFR 866.3120
Review panel
MI
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1983-05-04 – 1992-02-19
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