LEG BAG— 510(k) K780878

Substantially Equivalent

Abco Dealers, Inc.

FDA 510(k) clearance K780878 for LEG BAG, Substantially Equivalent on 1978-07-31. Applicant: Abco Dealers, Inc..

Clearance details

Applicant: Abco Dealers, Inc.
Product code: Code KNX
Advisory panel: Gastroenterology, Urology
Date received: 1978-05-30
Decision date: 1978-07-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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.