K862251

Substantially Equivalent

MODIFIED BIO-FLOW MODEL 200 URINE FLOW DEVICE

Applicant: Bio-Flow, Inc.
Product code: KNX
Advisory panel: Gastroenterology, Urology
Date received: 1986-06-12
Decision date: 1986-09-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Costa Mesa, CA, 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.