E-Z-Em, Inc.

FDA 510(k) & PMA Approved Devices — 56 products

Total Devices56

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K071378	MODIFICATION TO EMPOWER CT/CTA INJECTOR SYSTEM, MODELS 9800/9900 PRODUCT SERIES	JAK	2007-06-13	View
510(k)	K062449	EMPOWERMR INJECTOR SYSTEM, MODEL 9730	IZQ	2007-04-13	View
510(k)	K063029	EMPOWER CT/CTA INJECTOR SYSTEM, MODEL 9800/9900	JAK	2006-11-02	View
510(k)	K053008	E-Z-EM ENDOSCOPIC CO2 REGULATOR	FCX	2005-12-27	View
510(k)	K041178	EMPOWER TRANSFER SET, (CAT. NO. 7725)	FPK	2004-07-16	View
510(k)	K031571	EMPOWERCTA INJECTOR SYSTEM, MODELS 9930 & 9910 & 9825	IZQ	2003-06-19	View
510(k)	K030854	PROTOCO2L COLON INSUFFLATOR WITH PERFORMANCE IMPROVEMENTS, MODEL 6400	FCX	2003-04-16	View
510(k)	K013219	PROTOCO2L INSUFFLATOR MODEL 6400	FCX	2002-02-19	View
510(k)	K011160	E-Z EM PERCUPUMP 2001 CT INJECTOR	JAK	2001-05-16	View
510(k)	K974621	PERCUPUMP II WITH EDA	DSB	1998-01-27	View
510(k)	K961845	PERCUPUMP II WITH EDA	DSB	1997-01-23	View
510(k)	K954926	HM-CAP CONTROL PANEL	LYR	1996-01-30	View
510(k)	K932055	PERCUPUMP II	FIH	1995-03-21	View
510(k)	K930581	E-Z-FLATE	FCX	1994-07-01	View
510(k)	K911349	E-Z-EM ENTEROCLYSIS CATHETER SET	EZK	1992-11-16	View
510(k)	K914987	HIGH PRESSURE CONNECTING SETS, MODIFICATION	DTL	1992-05-20	View
510(k)	K914984	E-Z-FLOW ANGIOGRAPHY CATHETERS, MODIFICATION	DQY	1992-05-20	View
510(k)	K914986	GUIDE WIRES, MODIFICATION	DQX	1992-05-20	View
510(k)	K921738	SONO-VU US(TM), MODIFICATION	HIO	1992-04-27	View
510(k)	K920816	PERCUGUIDE LESION MARKING	GDF	1992-04-21	View