meddevicedb.com FDA Device Reference

T.E.D. SEQUENTIAL COMPRESSION SLEEVES

K781357 Class II Traditional
Decision Date
1978-09-20
Sponsor / Applicant
Kendall Research Center

Technical Specification

510(k) Submission ID K781357
Product Code JOW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5800
Decision Date 1978-09-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

T.E.D. SEQUENTIAL COMPRESSION SLEEVES received FDA 510(k) clearance under submission number K781357, sponsored by Kendall Research Center. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1978-09-20.

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.