K101900

Substantially Equivalent

HAKKI URINARY CATHETER; SIZE 14, 16, 18, 20, 22, 24, 26 FRENCH

Applicant: Hakki Medical Technologies, Inc.
Product code: GBM
Advisory panel: Gastroenterology, Urology
Date received: 2010-07-07
Decision date: 2011-02-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pinellas Park, FL, US

Adverse events under product code GBM

product code GBM

Injury: 397
Malfunction: 1,404
Total: 1,801

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.