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RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEM

K904237 Class I Traditional
Decision Date
1991-05-09
Sponsor / Applicant
Innovative Medical Technologies, Inc.

Technical Specification

510(k) Submission ID K904237
Product Code FPP
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6900
Decision Date 1991-05-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEM received FDA 510(k) clearance under submission number K904237, sponsored by Innovative Medical Technologies, Inc.. 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 1991-05-09.

Classification & Regulation

This clearance is catalogued under FDA product code FPP and 21 CFR 880.6900, within the General Hospital review panel as a Class I device.