K770672

Substantially Equivalent

COLLECTOR, SANI-CATCH, NO. 1010

Applicant: Concord Laboratories, Inc.
Product code: KNX
Advisory panel: Gastroenterology, Urology
Date received: 1977-04-08
Decision date: 1977-04-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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.