READYCATH CATHETER— 510(k) K973120

Substantially Equivalent

Medical Technologies of Georgia

FDA 510(k) clearance K973120 for READYCATH CATHETER, Substantially Equivalent on 1998-02-25. Applicant: Medical Technologies of Georgia.

Clearance details

Applicant: Medical Technologies of Georgia
Product code: Code GBM
Advisory panel: Gastroenterology, Urology
Date received: 1997-08-20
Decision date: 1998-02-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Decatur, GA, 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.