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

FISHER DIAGNOSTICS LATEST-CRP TEST KIT

K Number: K850160 · Decision Apr 19, 1985
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
125
Applicant Total
16
Review Days
94

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Basic Information

Device Name
FISHER DIAGNOSTICS LATEST-CRP TEST KIT
K Number
K850160
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5270
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Fisher Diagnostics
Date Received
January 15, 1985
Decision Date
April 19, 1985
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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Other Clearances by Fisher Diagnostics

K Number Device Name
K170652 ARCHITECT B.R.A.H.M.S PCT, ARCHITECT B.R.A.H.M.S PCT Calibrators, ARCHITECT B.R.A.H.M.S PCT Controls
K070640 ARCHITECT STAT TROPONIN-1; MYOGLOBIN
K052407 ARCHITECT ANTI-TPO IMMUNOASSAY, CALIBRATORS & CONTROLS
K052308 ARCHITECT ANTI-TG IMMUNOASSAY REAGENTS, CALIBRATORS, CONTROLS AND SYSTEM ASSAY CD-ROM
K042924 ARCHITECT STAT MYO IMMUNOASSAY
K041192 ARCHITECT STAT TROPONIN-I IMMUNOASSAY
K041596 ARCHITECT STAT CK-MB IMMUNOASSAY
K023362 FISHER DIAGNOSTICS THROMBOSCREEN 1000; PACIFIC HEMOSTASIS FIBRINOGEN REAGENT PLUS KAOLIN
K013397 PACIFIC HEMOSTASIS REFERENCE EMULSION
K010750 PACIFIC HEMOSTASIS INR CONTROL PLASMAS, MODEL CATALOG 100560
Search all 16 clearances from Fisher Diagnostics →