FDA 510(k) Application Details - K011725

Device Classification Name	Apparatus, Suction, Ward Use, Portable, Ac-Powered   More FDA Info for this Device
510(K) Number	K011725
Device Name	Apparatus, Suction, Ward Use, Portable, Ac-Powered
Applicant	KEYMED (MEDICAL & INDUSTRIAL EQUIPMENT), LTD. STOCK RD. SOUTHEND-ON-SEA, ESSEX SS25QH GB Other 510(k) Applications for this Company
Contact	ROGER GRAY 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	06/04/2001
Decision Date	08/31/2001
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