URINARY CATHETERIZATION SYSTEM W/O FOLEY— 510(k) K780831

Substantially Equivalent

Medical Devices, Inc.

FDA 510(k) clearance K780831 for URINARY CATHETERIZATION SYSTEM W/O FOLEY, Substantially Equivalent on 1978-07-27. Applicant: Medical Devices, Inc..

Clearance details

Applicant: Medical Devices, Inc.
Product code: Code KNX
Advisory panel: Gastroenterology, Urology
Date received: 1978-05-22
Decision date: 1978-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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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.