LAPAROSCOPIC LASER FIBER DIVERTER— 510(k) K912502

Substantially Equivalent

United States Endoscopy Group, Inc.

FDA 510(k) clearance K912502 for LAPAROSCOPIC LASER FIBER DIVERTER, Substantially Equivalent on 1991-07-25. Applicant: United States Endoscopy Group, Inc..

Clearance details

Applicant: United States Endoscopy Group, Inc.
Product code: Code GCJ
Advisory panel: Gastroenterology, Urology
Date received: 1991-06-05
Decision date: 1991-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mentor, OH, US

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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.