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

HEMOGLOBIN A1C REAGENT SET

K Number: K031539 · Decision Aug 6, 2003
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
248
Applicant Total
74
Review Days
82

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Basic Information

Device Name
HEMOGLOBIN A1C REAGENT SET
K Number
K031539
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7470
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Pointe Scientific, Inc.,
Date Received
May 16, 2003
Decision Date
August 6, 2003
Product Code
LCP
Advisory Committee
Hematology
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
LCP Assay, Glycosylated Hemoglobin

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K070504 AMMONIA/ALCOHOL CONTROL SET
K061377 APOLIPOPROTEIN A1 AND APOLIPOPROTEIN B REAGENTS AND CALIBRATORS
K051646 ISE DILUENT, 1N KCL, INTERNAL REFERENCE AND ISE STANDARDS LOW AND HIGH
K040391 TOTAL BILIRUBIN REAGENT SET
K023860 MICROALBUMIN REAGENT SET AND CALIBRATORS
K024006 G6PDH, GLUCOSE-6-PHOSHATE DEHYDROGENASE
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