STEALTH DILATION CATHETER SYSTEM (MODIFIED)— 510(k) K915895

Substantially Equivalent

Target Therapeutics

FDA 510(k) clearance K915895 for STEALTH DILATION CATHETER SYSTEM (MODIFIED), Substantially Equivalent on 1992-06-04. Applicant: Target Therapeutics.

Clearance details

Applicant: Target Therapeutics
Product code: Code LIT
Advisory panel: Cardiovascular
Date received: 1991-07-17
Decision date: 1992-06-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Jose, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code LIT

product code LIT

Death: 27
Injury: 1,256
Malfunction: 12,127
Total: 13,410

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.