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RESTORE, THERMACELLS (HOT PACK I)

K953442 Class I Traditional
Decision Date
1995-10-31
Sponsor / Applicant
Neal Dunning Assoc., Inc.

Technical Specification

510(k) Submission ID K953442
Product Code IMD
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5710
Decision Date 1995-10-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RESTORE, THERMACELLS (HOT PACK I) received FDA 510(k) clearance under submission number K953442, sponsored by Neal Dunning Assoc., 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 1995-10-31.

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.