meddevicedb.com FDA Device Reference

TORBOT VASCULAR COMPRESSION GARMENTS

K061411 Class II Traditional
Decision Date
2006-10-18
Sponsor / Applicant
Torbut Group, Inc.

Technical Specification

510(k) Submission ID K061411
Product Code DWL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5780
Decision Date 2006-10-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TORBOT VASCULAR COMPRESSION GARMENTS received FDA 510(k) clearance under submission number K061411, sponsored by Torbut Group, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2006-10-18.

Classification & Regulation

This clearance is catalogued under FDA product code DWL and 21 CFR 880.5780, within the General Hospital review panel as a Class II device.