FDA 510(k) Application Details - K042349

Device Classification Name	Apparatus, Suction, Ward Use, Portable, Ac-Powered   More FDA Info for this Device
510(K) Number	K042349
Device Name	Apparatus, Suction, Ward Use, Portable, Ac-Powered
Applicant	EMG TECHNOLOGY CO., LTD. 914 WEST PATAPSCO AVE. BALTIMORE, MD 21230 US Other 510(k) Applications for this Company
Contact	LEONARD FRIER 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	08/30/2004
Decision Date	12/16/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review