The following data is part of a premarket notification filed by Diagnostic Specialties with the FDA for Glucose Enzyme-color Reagent Set.
Device ID | K813412 |
510k Number | K813412 |
Device Name: | GLUCOSE ENZYME-COLOR REAGENT SET |
Classification | Glucose Oxidase, Glucose |
Applicant | DIAGNOSTIC SPECIALTIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | CGA |
CFR Regulation Number | 862.1345 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1981-12-04 |
Decision Date | 1981-12-31 |