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

K-ASSAY HS-CRP CONTROLS

K Number: K011079 · Decision May 16, 2001
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
125
Applicant Total
43
Review Days
37

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Basic Information

Device Name
K-ASSAY HS-CRP CONTROLS
K Number
K011079
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5270
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Kamiya Biomedical Co.
Date Received
April 9, 2001
Decision Date
May 16, 2001
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

Similar 510(k) Clearances

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

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Other Clearances by Kamiya Biomedical Co.

K Number Device Name
K093137 K-ASSAY CYSTATIN C REAGENT, CALIBRATOR AND CONTROL
K091486 K-ASSAY MICROALBUMIN AND K-ASSAY MICROALBUMIN CALIBRATOR
K050944 K-ASSAY FERRITIN (2) & FERRITIN CALIBRATOR SET
K042241 K-ASSAY TOTAL IGE, K-ASSAY IGE CALIBRATOR SET, MODELS KAI-092/KAI-093C
K030687 K-ASSAY D-DIMER, K-ASSAY D-DIMER CALIBRATOR, MODELS KAI-090; KAJ-091C
K023828 K-ASSAY C-REACTIVE PROTEIN (3), K-ASSAY CRP MULTI-CALIBRATOR D, K-ASSAY CRP MULTI-CALIBRATOR E, K-ASSAY CRP MULTI-CALIBR
K023853 K-ASSAY LP(A) CONTROLS
K022486 K-ASSAY HS-CRP CONTROLS
K021660 K-ASSAY LP(A) ASSAY
K014293 K-ASSAY FERRITIN, K-ASSAY FERRITIN CALIBRATOR SET
Search all 43 clearances from Kamiya Biomedical Co. →