meddevicedb.com FDA Device Reference

THERA-FIT

K930821 Class II Traditional
Decision Date
1994-11-09
Sponsor / Applicant
Aquatherapy Systems, Inc.

Technical Specification

510(k) Submission ID K930821
Product Code ILJ
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5100
Decision Date 1994-11-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THERA-FIT received FDA 510(k) clearance under submission number K930821, sponsored by Aquatherapy Systems, 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 1994-11-09.

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.