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

VITAMIN B12 RADIOASSAY

K Number: K780799 · Decision Jun 13, 1978
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
77
Applicant Total
94
Review Days
29

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Basic Information

Device Name
VITAMIN B12 RADIOASSAY
K Number
K780799
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1810
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Amersham Corp.
Date Received
May 15, 1978
Decision Date
June 13, 1978
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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