meddevicedb.com FDA Device Reference

READY-HEAT BLANKET

K042145 Class I Traditional
Decision Date
2004-09-17
Sponsor / Applicant
Techtrade, LLC

Technical Specification

510(k) Submission ID K042145
Product Code KME
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6060
Decision Date 2004-09-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

READY-HEAT BLANKET received FDA 510(k) clearance under submission number K042145, sponsored by Techtrade, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2004-09-17.

Classification & Regulation

This clearance is catalogued under FDA product code KME and 21 CFR 880.6060, within the General Hospital review panel as a Class I device.