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

IMMULITE 2500 VITAMIN B12 MODEL L5KVB2-200 TEST,L5KVB6-600 TEST, IMMULITE 2500 FOLIC ACID MODEL L5KFO2-200 TEST,L5KFO6-6

K Number: K060929 · Decision Apr 28, 2006
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
77
Applicant Total
3
Review Days
23

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Basic Information

Device Name
IMMULITE 2500 VITAMIN B12 MODEL L5KVB2-200 TEST,L5KVB6-600 TEST, IMMULITE 2500 FOLIC ACID MODEL L5KFO2-200 TEST,L5KFO6-6
K Number
K060929
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
862.1810
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Diagnostic Products Corporation
Date Received
April 5, 2006
Decision Date
April 28, 2006
Product Code
CDD
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
CDD Radioassay, Vitamin B12

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Other Clearances by Diagnostic Products Corporation

K Number Device Name
K063057 IMMULITE/IMMULITE 1000, IMMULITE 2000 HIGH SENSITIVITY CRP
K053533 IMMULITE/IMMULITE 1000 TURBO INTACT PTH