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

IMMUNO-CRP

K Number: K834390 · Decision Feb 3, 1984
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
69
Applicant Total
11
Review Days
51

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Basic Information

Device Name
IMMUNO-CRP
K Number
K834390
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5270
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Immunostics Co., Inc.
Date Received
December 14, 1983
Decision Date
February 3, 1984
Product Code
DCN
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
DCN System, Test, C-Reactive Protein

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DCN), ordered by most recent decision date.

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Other Clearances by Immunostics Co., Inc.

K Number Device Name
K926569 IMMUNO RA UNDILUTED
K902360 HEMA-SCREEN
K894780 IMMUNO/ASO
K883685 IMMUNO/FEBRILE ANTIGENS
K872910 IMMUNO/SLE
K863741 IMMUNO-CEPT D (BETA-MONOCLONAL)
K854619 DETECTACULT
K853105 IMMUNO-IM
K842110 SLIDE PREGNANCY TEST
K834391 IMMUNO-RA
Search all 11 clearances from Immunostics Co., Inc. →