510(k) K953196

CARDIO-SYSTEMS PRO-OP by Ch Administration, Inc. — Product Code FNM

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 8, 1995
Date Received
July 6, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mattress, Air Flotation, Alternating Pressure
Device Class
Class II
Regulation Number
880.5550
Review Panel
HO
Submission Type