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

TEST, SLIDE FOR C-REATIVE PROTEIN

K Number: K760354 · Decision Aug 11, 1976
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
125
Applicant Total
48
Review Days
9

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Basic Information

Device Name
TEST, SLIDE FOR C-REATIVE PROTEIN
K Number
K760354
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5270
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Icl Scientific
Date Received
August 2, 1976
Decision Date
August 11, 1976
Product Code
DCK
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
DCK C-Reactive Protein, Antigen, Antiserum, And Control

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K833761 THERAPEUTIC DRUG CONTROL
K832823 ENZYMUNE-TEST TSH
K831383 EVENT-TEST SLIDE
K823199 ENZYME-TEST DIGOXIN
K822346 HISTIMUNE ENZYME-ANA TEST
K822777 THERAPEUTIC DRUG CONTROL
K822465 ENZYMUNE SYSTEM I
K821374 ENZYMUNE-TEST INSULIN
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