GLUCOSE OXIDASE (FRINDER) KIT— 510(k) K791869

Name: FDA 510(k) clearance K791869
Creator: U.S. Food and Drug Administration
Published: 1979-10-01

Substantially Equivalent

Mid Tech, Inc.

FDA 510(k) clearance K791869 for GLUCOSE OXIDASE (FRINDER) KIT, Substantially Equivalent on 1979-10-01. Applicant: Mid Tech, Inc.. Device class: 2.

Clearance details

Applicant: Mid Tech, Inc.
Product code: Code CGA
Device class: Class 2
Regulation: 21 CFR 862.1345
Advisory panel: Clinical Chemistry
Date received: 1979-09-20
Decision date: 1979-10-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code CGA

product code CGA

Death: 2
Malfunction: 1,816
Total: 1,818

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.