CONVEEN INTERMITTENT CATHETERS— 510(k) K895548

Substantially Equivalent

Coloplast A/S

FDA 510(k) clearance K895548 for CONVEEN INTERMITTENT CATHETERS, Substantially Equivalent on 1990-02-09. Applicant: Coloplast A/S.

Clearance details

Applicant: Coloplast A/S
Product code: Code KOD
Advisory panel: Gastroenterology, Urology
Date received: 1989-09-13
Decision date: 1990-02-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Woth, TX, US

Download summary PDF View on FDA.gov ↗

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.