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

NYCOCARD CRP

K Number: K013787 · Decision May 14, 2002
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
125
Applicant Total
11
Review Days
181

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Basic Information

Device Name
NYCOCARD CRP
K Number
K013787
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5270
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Primus Corp.
Date Received
November 14, 2001
Decision Date
May 14, 2002
Product Code
DCK
Advisory Committee
Immunology
Review Advisory Committee
CH
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 Primus Corp.

K Number Device Name
K062658 PRIMUS A1CARE ASSAY
K014084 NYCOCARD CRP CONTROL
K994045 PRIMUS LIQUID CALIBRATOR FOR GHB/A1C LEVEL 1 AND LEVEL 2
K992921 PRIMUS LIQUID CONTROL FOR GHB/ALC LEVEL I AND LEVEL II
K955283 PRIMUS VARIANT SYSTEM PVS99
K942009 PRIMUS RAPID GEL 100 GLYCATED HEMOGLOBIN ASSAY
K940008 GLYCATED PROTEIN CALIBRATORS
K940142 GLYCATED PROTEIN CONTROLS
K936204 GLYCATED HEMOGLOBIN CALIBRATORS
K940143 GLYCATED HEMOGLOBIN CONTROLS
Search all 11 clearances from Primus Corp. →