FDA 510(k) Application Details - K961129

Device Classification Name	Mattress, Air Flotation, Alternating Pressure   More FDA Info for this Device
510(K) Number	K961129
Device Name	Mattress, Air Flotation, Alternating Pressure
Applicant	MELLEN AIR MFG., INC. 2840 TEMPLE AVE. LONG BEACH, CA 90806 US Other 510(k) Applications for this Company
Contact	BERTRAND H WEIDBERG Other 510(k) Applications for this Contact
Regulation Number	880.5550   More FDA Info for this Regulation Number
Classification Product Code	FNM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/21/1996
Decision Date	04/17/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review