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

CENTRIA RADIOIMMUNOASSAY SEPARATION

K Number: K792636 · Decision Jan 11, 1980
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
3
Applicant Total
69
Review Days
22

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Basic Information

Device Name
CENTRIA RADIOIMMUNOASSAY SEPARATION
K Number
K792636
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5510
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Union Carbide Corp.
Date Received
December 20, 1979
Decision Date
January 11, 1980
Product Code
KTS
Advisory Committee
Immunology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
KTS Second Antibody (Species Specific Anti-Animal Gamma Globulin)

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K812536 LINDE MARK II
K810732 LINDE MARK II OXYGEN RESERV. TYPE OR-4
K810596 CENTRIFI CHEM SYSTEM 400 ANALYZER
K810129 CENTRIFICHEM SYSTEM 500
K803216 CENTRIFICHEM AST/SGOT OPTIMIZED REAGENT
K802741 CENTRIFICHEM COMB. SERUM-BASED CALIB.
K802520 CENTRIFICHEM PIPETTOR ACCURACY CALIB.
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