VCARE DX— 510(k) K093556

Substantially Equivalent

Conmed Corporation

FDA 510(k) clearance K093556 for VCARE DX, Substantially Equivalent on 2010-03-12. Applicant: Conmed Corporation.

Clearance details

Applicant: Conmed Corporation
Product code: Code LKF
Advisory panel: Obstetrics/Gynecology
Date received: 2009-11-17
Decision date: 2010-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Utica, NY, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code LKF

product code LKF

Malfunction: 643
Other: 2
Total: 645

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.