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Antisera, If, Toxoplasma Gondii

FDA product code LJK · 6 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
1982-10-27 – 1997-12-11
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