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

ABBOTT AXSYM FOLATE

K Number: K972232 · Decision Jun 24, 1997
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
63
Applicant Total
857
Review Days
8

Basic Information

Device Name
ABBOTT AXSYM FOLATE
K Number
K972232
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1295
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ABBOTT LABORATORIES
Date Received
June 16, 1997
Decision Date
June 24, 1997
Product Code
CGN
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
CGN Acid, Folic, Radioimmunoassay

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