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

IMMULITE/IMMULITE 1000, IMMULITE 2000 HIGH SENSITIVITY CRP

K Number: K063057 · Decision Dec 22, 2006
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
18
Applicant Total
3
Review Days
78

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Basic Information

Device Name
IMMULITE/IMMULITE 1000, IMMULITE 2000 HIGH SENSITIVITY CRP
K Number
K063057
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
866.5270
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Diagnostic Products Corporation
Date Received
October 5, 2006
Decision Date
December 22, 2006
Product Code
NQD
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
NQD Cardiac C-Reactive Protein, Antigen, Antiserum, And Control

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

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Other Clearances by Diagnostic Products Corporation

K Number Device Name
K060929 IMMULITE 2500 VITAMIN B12 MODEL L5KVB2-200 TEST,L5KVB6-600 TEST, IMMULITE 2500 FOLIC ACID MODEL L5KFO2-200 TEST,L5KFO6-6
K053533 IMMULITE/IMMULITE 1000 TURBO INTACT PTH