meddevicedb.com FDA Device Reference

CLENSICAIR LOW AIRLOSS HYDROTHERAPY

K941610 Class II Traditional
Decision Date
1995-02-10
Sponsor / Applicant
Support Systems Intl.

Technical Specification

510(k) Submission ID K941610
Product Code IOQ
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5170
Decision Date 1995-02-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLENSICAIR LOW AIRLOSS HYDROTHERAPY received FDA 510(k) clearance under submission number K941610, sponsored by Support Systems Intl.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1995-02-10.

Classification & Regulation

This clearance is catalogued under FDA product code IOQ and 21 CFR 890.5170, within the Physical Medicine review panel as a Class II device.