FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

AMIZYME-TOXOPLASMA GONDII KIT

K Number: K842528 · Decision Sep 7, 1984
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
105
Applicant Total
32
Review Days
71

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Basic Information

Device Name
AMIZYME-TOXOPLASMA GONDII KIT
K Number
K842528
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3780
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Amico Lab, Inc.
Date Received
June 28, 1984
Decision Date
September 7, 1984
Product Code
LGD
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LGD Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii

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Other Clearances by Amico Lab, Inc.

K Number Device Name
K842662 ANTI-EPSTEIN-BARR VIRUS KIT
K842530 AMIZYME-EBV TEST KIT
K842663 ANTI-HERPES SIMPLEX VIRUS TYPE 1 OR 2
K842531 AMIZYME-HSV TYPES 1 & 2 TEST KITS
K842529 AMIZYME-CMV KIT
K842661 ANTI-CYTOMEGALOVIRUS KIT
K842660 ANTI-SCHISTOSOMA SPECIES KIT
K842658 ANTI-CHLAMYDIA TRACHOMATIS KIT
K842525 AMIZYME-C TRACHOMATIS TEST KIT
K842532 AMIZYME-ANA TEST KIT
Search all 32 clearances from Amico Lab, Inc. →