FDA 510(k) Application Details - K140031

Device Classification Name	Apparatus, Suction, Ward Use, Portable, Ac-Powered   More FDA Info for this Device
510(K) Number	K140031
Device Name	Apparatus, Suction, Ward Use, Portable, Ac-Powered
Applicant	DING HWA CO., LTD 1083 DELAWARE AVE. BUFFALO, NY 14223 US Other 510(k) Applications for this Company
Contact	ROBERT O DEAN 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	01/06/2014
Decision Date	04/28/2014
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review