meddevicedb.com FDA Device Reference

MODEL TURN Q PLUS AUTOMATIC TURNING MATTRESS WITH LOW AIR LOSS THERAPY

K950681 Class II Traditional
Decision Date
1995-05-16
Sponsor / Applicant
Invacare Corp.

Technical Specification

510(k) Submission ID K950681
Product Code IKZ
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5225
Decision Date 1995-05-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL TURN Q PLUS AUTOMATIC TURNING MATTRESS WITH LOW AIR LOSS THERAPY received FDA 510(k) clearance under submission number K950681, sponsored by Invacare Corp.. 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 1995-05-16.

Classification & Regulation

This clearance is catalogued under FDA product code IKZ and 21 CFR 890.5225, within the Physical Medicine review panel as a Class II device.