meddevicedb.com FDA Device Reference

PORTABLE SHOWER BATH

K823327 Class II Traditional
Decision Date
1982-12-07
Sponsor / Applicant
Wall Manufacturer, Inc.

Technical Specification

510(k) Submission ID K823327
Product Code ILM
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5100
Decision Date 1982-12-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PORTABLE SHOWER BATH received FDA 510(k) clearance under submission number K823327, sponsored by Wall Manufacturer, 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 1982-12-07.

Classification & Regulation

This clearance is catalogued under FDA product code ILM and 21 CFR 890.5100, within the Physical Medicine review panel as a Class II device.