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

ANTISERUM TO HUMAN IGM

K Number: K822670 · Decision Nov 17, 1982
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
62
Applicant Total
32
Review Days
75

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Basic Information

Device Name
ANTISERUM TO HUMAN IGM
K Number
K822670
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5550
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Amico Lab, Inc.
Date Received
September 3, 1982
Decision Date
November 17, 1982
Product Code
DFH
Advisory Committee
Immunology
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
DFH Kappa, Antigen, Antiserum, Control

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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. →