MERITEC-STREP GROUP A BETA-HEMOLYTIC— 510(k) K831599

Name: FDA 510(k) clearance K831599
Creator: U.S. Food and Drug Administration
Published: 1983-08-11

Substantially Equivalent

Meridian Diagnostics, Inc.

FDA 510(k) clearance K831599 for MERITEC-STREP GROUP A BETA-HEMOLYTIC, Substantially Equivalent on 1983-08-11. Applicant: Meridian Diagnostics, Inc.. Device class: 1.

Clearance details

Applicant: Meridian Diagnostics, Inc.
Product code: Code GTY
Device class: Class 1
Regulation: 21 CFR 866.3740
Advisory panel: Microbiology
Date received: 1983-05-17
Decision date: 1983-08-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code GTY

product code GTY

Death: 2
Total: 2

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.