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

K-ASSAY MULTI-ANALYTE CALIBRATOR

K Number: K993853 · Decision Dec 27, 1999
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
301
Applicant Total
43
Review Days
45

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Basic Information

Device Name
K-ASSAY MULTI-ANALYTE CALIBRATOR
K Number
K993853
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Kamiya Biomedical Co.
Date Received
November 12, 1999
Decision Date
December 27, 1999
Product Code
JIX
Advisory Committee
Clinical Chemistry
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
JIX Calibrator, Multi-Analyte Mixture

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JIX), 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. →