FDA 510(k) Application Details - K963558

Device Classification Name	Apparatus, Suction, Ward Use, Portable, Ac-Powered   More FDA Info for this Device
510(K) Number	K963558
Device Name	Apparatus, Suction, Ward Use, Portable, Ac-Powered
Applicant	CONTEMPORARY PRODUCTS, INC. 530 RIVERSIDE INDUSTRIAL PWKY. PORTLAND, ME 04103-1066 US Other 510(k) Applications for this Company
Contact	BARRY A SCHWARTZ Other 510(k) Applications for this Contact
Regulation Number	878.4780   More FDA Info for this Regulation Number
Classification Product Code	JCX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/05/1996
Decision Date	12/04/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review