meddevicedb.com FDA Device Reference

MALIBU BATHING SYSTEM

K925195 Class II Traditional
Decision Date
1994-10-17
Sponsor / Applicant
Medi-Man Rehabilitation Products, Inc.

Technical Specification

510(k) Submission ID K925195
Product Code ILJ
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5100
Decision Date 1994-10-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MALIBU BATHING SYSTEM received FDA 510(k) clearance under submission number K925195, sponsored by Medi-Man Rehabilitation Products, 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 1994-10-17.

Classification & Regulation

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