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

K-ASSAY MICROALBUMIN AND K-ASSAY MICROALBUMIN CALIBRATOR

K Number: K091486 · Decision Apr 29, 2010
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
36
Applicant Total
43
Review Days
345

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Basic Information

Device Name
K-ASSAY MICROALBUMIN AND K-ASSAY MICROALBUMIN CALIBRATOR
K Number
K091486
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5040
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Kamiya Biomedical Co.
Date Received
May 19, 2009
Decision Date
April 29, 2010
Product Code
DCF
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
DCF Albumin, Antigen, Antiserum, Control

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Other Clearances by Kamiya Biomedical Co.

K Number Device Name
K093137 K-ASSAY CYSTATIN C REAGENT, CALIBRATOR AND CONTROL
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
K012422 K-ASSAY D-DIMER CONTROLS
Search all 43 clearances from Kamiya Biomedical Co. →