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

ABNORMAL GLYCOSYLATED HEMOGLOBIN CONTROL

K Number: K811000 · Decision May 8, 1981
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
248
Applicant Total
111
Review Days
25

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Basic Information

Device Name
ABNORMAL GLYCOSYLATED HEMOGLOBIN CONTROL
K Number
K811000
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7470
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Corning Medical & Scientific
Date Received
April 13, 1981
Decision Date
May 8, 1981
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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