meddevicedb.com FDA Device Reference

ACTIVECARE SFT

K110159 Class II Traditional
Decision Date
2011-05-12
Sponsor / Applicant
Medical Compression Systems (Dbn) , Ltd.

Technical Specification

510(k) Submission ID K110159
Product Code JOW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5800
Decision Date 2011-05-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACTIVECARE SFT received FDA 510(k) clearance under submission number K110159, sponsored by Medical Compression Systems (Dbn) , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2011-05-12.

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.