Research Medical, Inc.

FDA 510(k) & PMA Approved Devices — 35 products

Total Devices35

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K970739	RMI HEMOCONCENTRATOR PREFERENCE PACK	KDI	1997-07-08	View
510(k)	K964833	RMI DUAL FLUID IRRIGATING SYRINGE	KYZ	1997-02-19	View
510(k)	K961927	RMI HEMOCONCENTRACTOR TUBING SET	DWF	1996-08-13	View
510(k)	K960098	RMI INTERNAL MAMMARY ARTERY CANNULA	DQR	1996-03-26	View
510(k)	K951344	RMI HEMOCONCENTRATOR	KDI	1995-08-15	View
510(k)	K922083	RMI SURGICCAL SITE VISUALIZATION WAND	FQH	1993-01-29	View
510(k)	K920936	RMI EXTERNAL CORONARY ARTERY OCCLUDER	DXC	1992-12-18	View
510(k)	K915869	RMI NORMOCLUDER CORONARY ARTERY OCCLUDER	MJN	1992-12-08	View
510(k)	K920676	RMI SOFCLAMP	DSS	1992-04-15	View
510(k)	K910221	RMI VASCULAR TOURNIQUET KIT	DXC	1991-05-16	View
510(k)	K901231	RMI CARDIOPLEGIA DELIVERY KITS	DWF	1990-06-08	View
510(k)	K897137	RMI AORTIC ROOT/CORONARY SINUS PRESSURE MONITORING	DTL	1990-03-27	View
510(k)	K896777	RMI AORTIC ROOT PRESSURE MONITOR EXTENSION LINE	DWF	1990-02-27	View
510(k)	K896778	RMI VASOPLEGIA CANNULA WITH & WITHOUT CHECK VALVE	DWF	1990-02-27	View
510(k)	K896636	RMI ANTEPLEGIA CANNULA	DWF	1990-02-15	View
510(k)	K892368	RMI CARDIOPLEGIA DELIVERY SETS	DTL	1989-12-07	View
510(k)	K892377	RMI AORTIC ROOT/CORONARY SINUS MONIT./INFUSION SET	DTL	1989-12-07	View
510(k)	K891576	FEM-FLEX FEMORAL ACCESS CANNULATION SET	DWF	1989-10-12	View
510(k)	K894243	RMI ARTERIAL PERFUSION CANNULA	DQR	1989-09-19	View
510(k)	K880103	CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPUL.	DWF	1988-03-22	View