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

K-ASSAY D-DIMER CONTROLS

K Number: K012422 · Decision Aug 21, 2001
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
39
Applicant Total
43
Review Days
22

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Basic Information

Device Name
K-ASSAY D-DIMER CONTROLS
K Number
K012422
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5425
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Kamiya Biomedical Co.
Date Received
July 30, 2001
Decision Date
August 21, 2001
Product Code
GGC
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GGC Control, Plasma, Abnormal

Similar 510(k) Clearances

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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. →