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

PROTEIN-BOUND GLUCOSE ASSAYN KIT

K Number: K930823 · Decision Aug 19, 1993
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
248
Applicant Total
8
Review Days
183

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Basic Information

Device Name
PROTEIN-BOUND GLUCOSE ASSAYN KIT
K Number
K930823
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7470
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Diagnostic Specialties
Date Received
February 17, 1993
Decision Date
August 19, 1993
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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