ALBERT MORTON UROLOGICAL CATHETER— 510(k) K901441

Substantially Equivalent

Transinternational Marketing Group

FDA 510(k) clearance K901441 for ALBERT MORTON UROLOGICAL CATHETER, Substantially Equivalent on 1990-06-22. Applicant: Transinternational Marketing Group.

Clearance details

Applicant: Transinternational Marketing Group
Product code: Code GBM
Advisory panel: Gastroenterology, Urology
Date received: 1990-03-27
Decision date: 1990-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Port Of Charleston, SC, US

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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.