Atlas FDA

Cardiogenes

20 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
ECLIPSE 2000 (K961560)Cardiogenes1997-01-27
ECLIPSE 2100 (K955006)Cardiogenes1996-01-17
POWERSCULPTOR PROBES (K952755)Cardiogenes1995-09-14
CORSSFIRE PLUS (K953658)Cardiogenes1995-08-21
ECLIPSE 3200 (K953424)Cardiogenes1995-08-11
ECLIPSE 3200 (K945126)Cardiogenes1995-01-18
SUNRISE TECHNOLOGIES MODEL 5020 PLDD KIT (K944758)Cardiogenes1994-12-27
ECLIPSE 3200 (K944153)Cardiogenes1994-11-09
OPTICAL FIBER FOR ENT APPLICATIONS (K944151)Cardiogenes1994-11-01
CROSSFIRE(TM) (705-10650) (K943171)Cardiogenes1994-09-20
ECLIPSE 3200 (K943311)Cardiogenes1994-07-22
ECLIPSE 3200 FOR USE IN UROLOGY APPLICATIONS (K931305)Cardiogenes1994-01-07
ECLIPSE LAZERBLADE(TM) FIBEROPTIC DELIVERY SYSTEM (K934935)Cardiogenes1993-11-22
ECLIPSE 2100(TM) MODEL 32, MODIFICATION (K931101)Cardiogenes1993-08-25
ECLIPSE 3200 (K926210)Cardiogenes1993-07-28
ECLIPSE 3200 FOR USE IN ORTHO SURG/ARTH APPL JOINT (K931306)Cardiogenes1993-07-23
ECLIPSE 3200 (K925840)Cardiogenes1993-06-25
ECLIPSE 3200(TM) HO:YAG LASER FOR PERCU DISKETOMY (K924943)Cardiogenes1993-05-17
ECLIPSE 2100(TM) MODEL 32 (K924214)Cardiogenes1992-11-16
ECLIPSE 2100 (K921038)Cardiogenes1992-06-04

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