FDA 510(k) Application Details - K962181

Device Classification Name	Stretcher, Wheeled   More FDA Info for this Device
510(K) Number	K962181
Device Name	Stretcher, Wheeled
Applicant	DYNA CORP. 6300 YARROW DR. CARLSBAD, CA 92009-1597 US Other 510(k) Applications for this Company
Contact	HENRY C PERRY Other 510(k) Applications for this Contact
Regulation Number	880.6910   More FDA Info for this Regulation Number
Classification Product Code	FPO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/06/1996
Decision Date	08/01/1996
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