VEIN ENTRY INDICATOR DEVICE (VEID)— 510(k) K993995

Substantially Equivalent

Vascular Technologies , Ltd.

FDA 510(k) clearance K993995 for VEIN ENTRY INDICATOR DEVICE (VEID), Substantially Equivalent on 2000-02-14. Applicant: Vascular Technologies , Ltd..

Clearance details

Applicant: Vascular Technologies , Ltd.
Product code: Code FMF
Advisory panel: General Hospital
Date received: 1999-11-24
Decision date: 2000-02-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ginot Shomron 44853, IL

Download summary PDF View on FDA.gov ↗

Adverse events under product code FMF

product code FMF

Death: 15
Injury: 2,263
Malfunction: 29,722
Other: 17
Total: 32,017

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.