REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS— 510(k) K022748

Substantially Equivalent

Medical Device Services

FDA 510(k) clearance K022748 for REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS, Substantially Equivalent on 2002-10-09. Applicant: Medical Device Services.

Clearance details

Applicant: Medical Device Services
Product code: Code HET
Advisory panel: Obstetrics/Gynecology
Date received: 2002-08-19
Decision date: 2002-10-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. George, UT, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code HET

product code HET

Malfunction: 10,504
Total: 10,504

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.