FDA 510(k) Applications Submitted by KEN RAICHMAN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K070212	01/22/2007	CITOP10 GUIDEWIRE, 0.014(1.4MM TIP), CITOP6 GUIDEWIRE, 0.014(1.0MM TIP), CITOP SUPPORT ACCESSORY, 0.023(126CM)	OVALUM LTD.
K001120	04/07/2000	ENVOY PATIENT MONITOR	MENNEN MEDICAL LTD.
K021981	06/17/2002	IVENT 201 PORTABLE VENTILATOR	VERSAMED LTD.
K011957	06/22/2001	IVENT 201 PORTABLE VENTILATOR	VERSAMED LTD.
K982697	08/03/1998	MODIFICATION TO ENSEMBLE CENTRAL STATION MONITOR	MENNEN MEDICAL, INC.
K000563	02/22/2000	MODIFICATION TO ENVOY PATIENT MONITOR	MENNEN MEDICAL LTD.
K991775	05/25/1999	MODIFICATION TO COMPUTERIZED CATHETERIZATION LABORATORY - HORIZON 9000 WS	MENNEN MEDICAL, INC.
K983864	11/02/1998	ETCO2 VITAL SIGNS MODULE	MENNEN MEDICAL, INC.
K974510	12/01/1997	ENVOY PATIENT MONITOR	MENNEN MEDICAL, INC.