Cardiogenes

FDA 510(k) & PMA Approved Devices — 20 products

Total Devices20

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K961560	ECLIPSE 2000	GEX	1997-01-27	View
510(k)	K955006	ECLIPSE 2100	GEX	1996-01-17	View
510(k)	K952755	POWERSCULPTOR PROBES	GEX	1995-09-14	View
510(k)	K953658	CORSSFIRE PLUS	GEX	1995-08-21	View
510(k)	K953424	ECLIPSE 3200	GEX	1995-08-11	View
510(k)	K945126	ECLIPSE 3200	GEX	1995-01-18	View
510(k)	K944758	SUNRISE TECHNOLOGIES MODEL 5020 PLDD KIT	GEX	1994-12-27	View
510(k)	K944153	ECLIPSE 3200	GEX	1994-11-09	View
510(k)	K944151	OPTICAL FIBER FOR ENT APPLICATIONS	GEX	1994-11-01	View
510(k)	K943171	CROSSFIRE(TM) (705-10650)	GEX	1994-09-20	View
510(k)	K943311	ECLIPSE 3200	GEX	1994-07-22	View
510(k)	K931305	ECLIPSE 3200 FOR USE IN UROLOGY APPLICATIONS	GEX	1994-01-07	View
510(k)	K934935	ECLIPSE LAZERBLADE(TM) FIBEROPTIC DELIVERY SYSTEM	GEX	1993-11-22	View
510(k)	K931101	ECLIPSE 2100(TM) MODEL 32, MODIFICATION	GEX	1993-08-25	View
510(k)	K926210	ECLIPSE 3200	GEX	1993-07-28	View
510(k)	K931306	ECLIPSE 3200 FOR USE IN ORTHO SURG/ARTH APPL JOINT	GEX	1993-07-23	View
510(k)	K925840	ECLIPSE 3200	GEX	1993-06-25	View
510(k)	K924943	ECLIPSE 3200(TM) HO:YAG LASER FOR PERCU DISKETOMY	GEX	1993-05-17	View
510(k)	K924214	ECLIPSE 2100(TM) MODEL 32	GEX	1992-11-16	View
510(k)	K921038	ECLIPSE 2100	GEX	1992-06-04	View