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

CEDIA (R) VITAMIN B12/FOLATE ASSAY

K Number: K904776 · Decision Nov 20, 1990
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
77
Applicant Total
107
Review Days
29

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Basic Information

Device Name
CEDIA (R) VITAMIN B12/FOLATE ASSAY
K Number
K904776
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1810
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Microgenics Corp.
Date Received
October 22, 1990
Decision Date
November 20, 1990
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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