meddevicedb.com FDA Device Reference

TMR-670

K931349 Class II Traditional
Decision Date
1993-07-22
Sponsor / Applicant
Pride Health Care, Inc.

Technical Specification

510(k) Submission ID K931349
Product Code INO
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3110
Decision Date 1993-07-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TMR-670 received FDA 510(k) clearance under submission number K931349, sponsored by Pride Health Care, 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 1993-07-22.

Classification & Regulation

This clearance is catalogued under FDA product code INO and 21 CFR 890.3110, within the Physical Medicine review panel as a Class II device.