FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

CRP (II) CALIBRATORS

K Number: K030546 · Decision Jun 2, 2003
Classifications
1
FEI Numbers
72
Registration Numbers
72
Same Product Code
129
Applicant Total
6
Review Days
102

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Basic Information

Device Name
CRP (II) CALIBRATORS
K Number
K030546
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Denka Seiken Co., Ltd.
Date Received
February 20, 2003
Decision Date
June 2, 2003
Product Code
JIS
Advisory Committee
Clinical Chemistry
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
JIS Calibrator, Primary

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K Number Device Name
K161679 s LDL-EX SEIKEN
K060359 ARCHIECT INSULIN AND CONTROLS, MODEL 8K41-01, 8K41-10
K043264 LDL-EX SEIKEN ASSAY KIT
K041090 HDL-EX SEIKEN ASSAY KIT
K030545 CRP-LATEX (II)X2 SEIKEN ASSAY KIT