Cleared Traditional

K904237 - RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEM
(FDA 510(k) Clearance)

K904237 · Innovative Medical Technologies, Inc. · General Hospital
May 1991
Decision
234d
Days
Class 1
Risk

K904237 is an FDA 510(k) clearance for the RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEM. This device is classified as a Stretcher, Hand-carried (Class I — General Controls, product code FPP).

Submitted by Innovative Medical Technologies, Inc. (V2c5a9, CA). The FDA issued a Cleared decision on May 9, 1991, 234 days after receiving the submission on September 17, 1990.

This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 880.6900.

Submission Details

510(k) Number K904237 FDA.gov
FDA Decision Cleared SESE
Date Received September 17, 1990
Decision Date May 09, 1991
Days to Decision 234 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary —

Device Classification

Product Code FPP — Stretcher, Hand-carried
Device Class Class I — General Controls
CFR Regulation 21 CFR 880.6900