ORIGIN SECONDARY CANNULA AND TROCAR— 510(k) K922460

Substantially Equivalent

Origin Medsystems, Inc.

FDA 510(k) clearance K922460 for ORIGIN SECONDARY CANNULA AND TROCAR, Substantially Equivalent on 1992-09-16. Applicant: Origin Medsystems, Inc..

Clearance details

Applicant: Origin Medsystems, Inc.
Product code: Code GEA
Advisory panel: General, Plastic Surgery
Date received: 1992-05-26
Decision date: 1992-09-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Carlos, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code GEA

product code GEA

Malfunction: 587
Total: 587

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.