FDA 510(k) Application Details - K102626

Device Classification Name	Apparatus, Suction, Ward Use, Portable, Ac-Powered   More FDA Info for this Device
510(K) Number	K102626
Device Name	Apparatus, Suction, Ward Use, Portable, Ac-Powered
Applicant	VEGA TECHNOLOGIES, INC. 11F-13, 100 CHANG-CHUN RD. TAIPEI 104 TW Other 510(k) Applications for this Company
Contact	JOSEPH LU 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	09/13/2010
Decision Date	11/12/2010
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