meddevicedb.com FDA Device Reference

ICE BAND

K771002 Class I Traditional
Decision Date
1977-08-30
Sponsor / Applicant
Norcliff Thayer, Inc.

Technical Specification

510(k) Submission ID K771002
Product Code IME
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5700
Decision Date 1977-08-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ICE BAND received FDA 510(k) clearance under submission number K771002, sponsored by Norcliff Thayer, 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 1977-08-30.

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.