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RECUMBENT BATHING SYSTEMS, RHAPSODY AND PRIMO

K001079 Class II Traditional
Decision Date
2000-05-01
Sponsor / Applicant
Arjo, Inc.

Technical Specification

510(k) Submission ID K001079
Product Code ILJ
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5100
Decision Date 2000-05-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RECUMBENT BATHING SYSTEMS, RHAPSODY AND PRIMO received FDA 510(k) clearance under submission number K001079, sponsored by Arjo, 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 2000-05-01.

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.