meddevicedb.com FDA Device Reference

REPROCESSED COMPRESSION SLEEVES

K100909 Class II Traditional
Decision Date
2010-07-23
Sponsor / Applicant
Ascent Healthcare Solutions

Technical Specification

510(k) Submission ID K100909
Product Code JOW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5800
Decision Date 2010-07-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REPROCESSED COMPRESSION SLEEVES received FDA 510(k) clearance under submission number K100909, sponsored by Ascent Healthcare Solutions. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2010-07-23.

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.