meddevicedb.com FDA Device Reference

LOW BACK POSTURE PILLOW

K802442 Class I Traditional
Decision Date
1980-10-31
Sponsor / Applicant
Body Therapeutics, Inc.

Technical Specification

510(k) Submission ID K802442
Product Code IQK
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3490
Decision Date 1980-10-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LOW BACK POSTURE PILLOW received FDA 510(k) clearance under submission number K802442, sponsored by Body Therapeutics, Inc.. 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 1980-10-31.

Classification & Regulation

This clearance is catalogued under FDA product code IQK and 21 CFR 890.3490, within the Physical Medicine review panel as a Class I device.