GLUCOSE STANDARD

Calibrator, Primary

ANCO MEDICAL REAGENTS & ASSOC.

The following data is part of a premarket notification filed by Anco Medical Reagents & Assoc. with the FDA for Glucose Standard.

Pre-market Notification Details

Device IDK810091
510k NumberK810091
Device Name:GLUCOSE STANDARD
ClassificationCalibrator, Primary
Applicant ANCO MEDICAL REAGENTS & ASSOC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeJIS  
CFR Regulation Number862.1150 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1981-01-13
Decision Date1981-01-26

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