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

A1C 2.2 PLUS - AUTOMATED GLYCOHEMOGLOBIN ANALYZER

K Number: K972265 · Decision Sep 25, 1997
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
248
Applicant Total
41
Review Days
100

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Basic Information

Device Name
A1C 2.2 PLUS - AUTOMATED GLYCOHEMOGLOBIN ANALYZER
K Number
K972265
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7470
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Tosoh Medics, Inc.
Date Received
June 17, 1997
Decision Date
September 25, 1997
Product Code
LCP
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LCP Assay, Glycosylated Hemoglobin

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