ULTRAFLEX ESOPHAGEAL NG STENT SYSTEM— 510(k) K032930

Substantially Equivalent

Boston Scientific Corp

FDA 510(k) clearance K032930 for ULTRAFLEX ESOPHAGEAL NG STENT SYSTEM, Substantially Equivalent on 2003-10-23. Applicant: Boston Scientific Corp.

Clearance details

Applicant: Boston Scientific Corp
Product code: Code ESW
Advisory panel: General, Plastic Surgery
Date received: 2003-09-22
Decision date: 2003-10-23
Decision: Substantially Equivalent
Clearance type: Special
Location: Natick,, MA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code ESW

product code ESW

Death: 11
Injury: 353
Malfunction: 442
Total: 806

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.