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FLOTATION THERAPY BED

K771264 Class II Traditional
Decision Date
1977-08-02
Sponsor / Applicant
Aquarius Medical Services

Technical Specification

510(k) Submission ID K771264
Product Code IOQ
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5170
Decision Date 1977-08-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLOTATION THERAPY BED received FDA 510(k) clearance under submission number K771264, sponsored by Aquarius Medical Services. 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 1977-08-02.

Classification & Regulation

This clearance is catalogued under FDA product code IOQ and 21 CFR 890.5170, within the Physical Medicine review panel as a Class II device.