URINARY DRAINAGE BAG— 510(k) K820136

Substantially Equivalent

Megaplast, Inc.

FDA 510(k) clearance K820136 for URINARY DRAINAGE BAG, Substantially Equivalent on 1982-01-29. Applicant: Megaplast, Inc..

Clearance details

Applicant: Megaplast, Inc.
Product code: Code KNX
Advisory panel: Gastroenterology, Urology
Date received: 1982-01-18
Decision date: 1982-01-29
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.