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WONDER WARMER

K810633 Class I Traditional
Decision Date
1981-03-26
Sponsor / Applicant
Montvale Products, Inc.

Technical Specification

510(k) Submission ID K810633
Product Code IMD
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5710
Decision Date 1981-03-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WONDER WARMER received FDA 510(k) clearance under submission number K810633, sponsored by Montvale Products, 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 1981-03-26.

Classification & Regulation

This clearance is catalogued under FDA product code IMD and 21 CFR 890.5710, within the Physical Medicine review panel as a Class I device.