LTFS230— 510(k) K021775

Substantially Equivalent

Healthtronics, Inc.

FDA 510(k) clearance K021775 for LTFS230, Substantially Equivalent on 2002-12-23. Applicant: Healthtronics, Inc..

Clearance details

Applicant: Healthtronics, Inc.
Product code: Code LNS
Advisory panel: Gastroenterology, Urology
Date received: 2002-05-29
Decision date: 2002-12-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Marietta, GA, US

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Adverse events under product code LNS

product code LNS

Death: 4
Injury: 320
Total: 324

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.