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Anti-Dna Indirect Immunofluorescent Solid Phase

FDA product code KTL · 19 cleared devices

Class 2 Immunology
Regulation
21 CFR 866.5100
Review panel
IM
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1979-09-17 – 2023-08-31
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