meddevicedb.com FDA Device Reference

HOTPAD

K915876 Class I Traditional
Decision Date
1993-02-12
Sponsor / Applicant
Ten Comfort Corp.

Technical Specification

510(k) Submission ID K915876
Product Code IME
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5700
Decision Date 1993-02-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HOTPAD received FDA 510(k) clearance under submission number K915876, sponsored by Ten Comfort Corp.. 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 1993-02-12.

Classification & Regulation

This clearance is catalogued under FDA product code IME and 21 CFR 890.5700, within the Physical Medicine review panel as a Class I device.