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Direct Agglutination Test, Toxoplasma Gondii

FDA product code LLA · 4 cleared devices

Class 2 Microbiology
Regulation
21 CFR 866.3780
Review panel
MI
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1983-09-26 – 1993-01-11
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