VACULINK, MODEL VCL 3000— 510(k) K043614

Substantially Equivalent

Medevco, Inc.

FDA 510(k) clearance K043614 for VACULINK, MODEL VCL 3000, Substantially Equivalent on 2005-04-14. Applicant: Medevco, Inc..

Clearance details

Applicant: Medevco, Inc.
Product code: Code HDB
Advisory panel: Obstetrics/Gynecology
Date received: 2004-12-30
Decision date: 2005-04-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Plano, TX, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code HDB

product code HDB

Death: 7
Total: 7

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.