meddevicedb.com FDA Device Reference

EZ VEIN INFLATABLE TOURNIQUET

K112874 Class I Traditional
Decision Date
2011-10-17
Sponsor / Applicant
Dominion Medical Devices, LLC

Technical Specification

510(k) Submission ID K112874
Product Code KCY
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5910
Decision Date 2011-10-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EZ VEIN INFLATABLE TOURNIQUET received FDA 510(k) clearance under submission number K112874, sponsored by Dominion Medical Devices, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2011-10-17.

Classification & Regulation

This clearance is catalogued under FDA product code KCY and 21 CFR 878.5910, within the General, Plastic Surgery review panel as a Class I device.