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

POINTE 750 GLYCOMETER

K Number: K920449 · Decision Jul 28, 1992
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
248
Applicant Total
74
Review Days
177

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Basic Information

Device Name
POINTE 750 GLYCOMETER
K Number
K920449
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
February 2, 1992
Decision Date
July 28, 1992
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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Other Clearances by Pointe Scientific, Inc.,

K Number Device Name
K070757 MICROPROTEIN REAGENT SET
K062118 POINTE 360
K070251 CARBON DIOXIDE LIQUID STABLE REAGENT
K070207 MULTI-ANALYTE CHEMISTRY CALIBRATOR
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
K031539 HEMOGLOBIN A1C REAGENT SET
K023860 MICROALBUMIN REAGENT SET AND CALIBRATORS
Search all 74 clearances from Pointe Scientific, Inc., →