CATHETER, MMG LATEX EXTERNAL— 510(k) K790279

Name: FDA 510(k) clearance K790279
Creator: U.S. Food and Drug Administration
Published: 1979-03-06

Substantially Equivalent

Medical Marketing Group

FDA 510(k) clearance K790279 for CATHETER, MMG LATEX EXTERNAL, Substantially Equivalent on 1979-03-06. Applicant: Medical Marketing Group. Device class: 2.

Clearance details

Applicant: Medical Marketing Group
Product code: Code KNX
Device class: Class 2
Regulation: 21 CFR 876.5250
Advisory panel: Gastroenterology, Urology
Date received: 1979-02-13
Decision date: 1979-03-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Decatur, GA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code KNX

product code KNX

Malfunction: 1,064
Total: 1,064

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.