meddevicedb.com FDA Device Reference

COMPRINET, COMTESSE AND BELLAVAR STOCKINGS

K905631 Class II Traditional
Decision Date
1991-03-07
Sponsor / Applicant
Jobst Institute, Inc.

Technical Specification

510(k) Submission ID K905631
Product Code DWL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5780
Decision Date 1991-03-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMPRINET, COMTESSE AND BELLAVAR STOCKINGS received FDA 510(k) clearance under submission number K905631, sponsored by Jobst Institute, 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 1991-03-07.

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.