510(k) K904237

RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEM by Innovative Medical Technologies, Inc. — Product Code FPP

K904237 is an FDA 510(k) premarket notification submitted by Innovative Medical Technologies, Inc. for the device "RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEM". The FDA issued a decision of Substantially Equivalent on May 9, 1991. The device falls under product code FPP (Stretcher, Hand-Carried), a Class I device regulated under 21 CFR 880.6900. Innovative Medical Technologies, Inc. has at least 5 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 9, 1991
Date Received
September 17, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stretcher, Hand-Carried
Device Class
Class I
Regulation Number
880.6900
Review Panel
HO
Submission Type