FDA 510(k) Applications for Medical Device Product Code: MDM (Instrument, Manual, Surgical, General Use)

FDA 510(k) Applications for Medical Device Product Code "MDM"
(Instrument, Manual, Surgical, General Use)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K023173	ANDREWS SURGICAL INNOVATIONS, LTD.	ANDREWS INTRODUCER, MODEL ASI01	12/18/2002
K022059	BOSTON SCIENTIFIC CORP.	MICROVASIVE PULMONARY GUIDEWIRE	11/13/2002
K010184	CANICA DESIGN, INC.	CHESS HAND SURGERY SYSTEM	06/22/2001
K981579	ETHICON, INC.	ENDOPOUCH PRO SPECIMEN RETRIEVAL BAG	07/09/1998
K050575	FUTUMEDS SDN BHD	FUTUMEDS NO PATIENT CONTACT SAFETY LANCET WITH PALS SYSTEM	08/15/2005
K990062	GENZYME SURGICAL PRODUCT (GENZYME BIOSURGERY)	SAPHLIFT	03/30/1999
K073664	INJECTIMED, INC.	FRONTLINE MEDICAL SAFETYNET GUIDEWIRE INTRODUCER	08/08/2008
K013040	MINRAD, INC.	LIGHT SABER INTRODUCER NEEDLE	12/07/2001
K050957	SPECIAL DEVICES, INC.	EUTROCHAR	05/18/2005