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Indirect Fluorescent Antibody Test, Entamoeba Histolytica & Rel Sp

FDA product code GWD · 2 cleared devices

Class 2 Microbiology
Regulation
21 CFR 866.3220
Review panel
MI
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1985-01-23 – 1987-09-16
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