meddevicedb.com FDA Device Reference

JACE MODEL T300 TOE CPM DEVICE

K913227 Class I Traditional
Decision Date
1991-08-16
Sponsor / Applicant
Thera Kinetics, Inc.

Technical Specification

510(k) Submission ID K913227
Product Code BXB
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5380
Decision Date 1991-08-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

JACE MODEL T300 TOE CPM DEVICE received FDA 510(k) clearance under submission number K913227, sponsored by Thera Kinetics, 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 1991-08-16.

Classification & Regulation

This clearance is catalogued under FDA product code BXB and 21 CFR 890.5380, within the Physical Medicine review panel as a Class I device.