LAGIS ENDOSCOPIC INSTRUMENTS DISPOSABLE GRASPER— 510(k) K141902

Substantially Equivalent

Lagis Enterprises Co, Ltd.

FDA 510(k) clearance K141902 for LAGIS ENDOSCOPIC INSTRUMENTS DISPOSABLE GRASPER, Substantially Equivalent on 2015-05-26. Applicant: Lagis Enterprises Co, Ltd..

Clearance details

Applicant: Lagis Enterprises Co, Ltd.
Product code: Code GCJ
Advisory panel: Gastroenterology, Urology
Date received: 2014-07-14
Decision date: 2015-05-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taichung, TW

Download summary PDF View on FDA.gov ↗

Adverse events under product code GCJ

product code GCJ

Death: 39
Injury: 1,638
Malfunction: 28,216
Other: 11
Total: 29,904

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.