meddevicedb.com FDA Device Reference

3M BRAND TOTAL LEG COMPRESSION TLC SYS.

K791894 Class II Traditional
Decision Date
1979-11-16
Sponsor / Applicant
3M Company

Technical Specification

510(k) Submission ID K791894
Product Code JOW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5800
Decision Date 1979-11-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

3M BRAND TOTAL LEG COMPRESSION TLC SYS. received FDA 510(k) clearance under submission number K791894, sponsored by 3M Company. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1979-11-16.

Classification & Regulation

This clearance is catalogued under FDA product code JOW and 21 CFR 870.5800, within the Cardiovascular review panel as a Class II device.