MMG CATHETER PLUG W/DRAINAGE TUBE COVER— 510(k) K874682

Name: FDA 510(k) clearance K874682
Creator: U.S. Food and Drug Administration
Published: 1988-01-27

Substantially Equivalent

Medical Marketing Group

FDA 510(k) clearance K874682 for MMG CATHETER PLUG W/DRAINAGE TUBE COVER, Substantially Equivalent on 1988-01-27. Applicant: Medical Marketing Group. Device class: 2.

Clearance details

Applicant: Medical Marketing Group
Product code: Code KOD
Device class: Class 2
Regulation: 21 CFR 876.5130
Advisory panel: Gastroenterology, Urology
Date received: 1987-11-13
Decision date: 1988-01-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Decatur, GA, US

Download summary PDF View on FDA.gov ↗

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K910022 — MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KIT1991-04-02
K884819 — O'NEIL URINARY CATHETER INTRODUCER1989-02-17
K871999 — MMG URO-SELF CATHETER1987-08-25
K863912 — THE MMG 5 IN 1 CONNECTOR1986-10-27
K840838 — MMG CONNECTIVE TUBING1984-03-30

Adverse events under product code KOD

product code KOD

Death: 5
Injury: 1,129
Malfunction: 7,019
Total: 8,153

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.