SNARE— 510(k) K960230

Substantially Equivalent

Lighthouse Medical, Inc.

FDA 510(k) clearance K960230 for SNARE, Substantially Equivalent on 1996-07-31. Applicant: Lighthouse Medical, Inc..

Clearance details

Applicant: Lighthouse Medical, Inc.
Product code: Code FDI
Advisory panel: Gastroenterology, Urology
Date received: 1996-01-17
Decision date: 1996-07-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waltham, MA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FDI

product code FDI

Death: 6
Injury: 217
Malfunction: 1,544
Total: 1,767

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.