Cardiogenes
Cardiogenes holds FDA 510(k) medical device clearances, first cleared 1992, most recent 1997.
Top product codes for Cardiogenes
Recent clearances by Cardiogenes
- K961560 — ECLIPSE 2000
- K955006 — ECLIPSE 2100
- K952755 — POWERSCULPTOR PROBES
- K953658 — CORSSFIRE PLUS
- K953424 — ECLIPSE 3200
- K945126 — ECLIPSE 3200
- K944758 — SUNRISE TECHNOLOGIES MODEL 5020 PLDD KIT
- K944153 — ECLIPSE 3200
- K944151 — OPTICAL FIBER FOR ENT APPLICATIONS
- K943171 — CROSSFIRE(TM) (705-10650)
- K943311 — ECLIPSE 3200
- K931305 — ECLIPSE 3200 FOR USE IN UROLOGY APPLICATIONS
- K934935 — ECLIPSE LAZERBLADE(TM) FIBEROPTIC DELIVERY SYSTEM
- K931101 — ECLIPSE 2100(TM) MODEL 32, MODIFICATION
- K926210 — ECLIPSE 3200
- K931306 — ECLIPSE 3200 FOR USE IN ORTHO SURG/ARTH APPL JOINT
- K925840 — ECLIPSE 3200
- K924943 — ECLIPSE 3200(TM) HO:YAG LASER FOR PERCU DISKETOMY
- K924214 — ECLIPSE 2100(TM) MODEL 32
- K921038 — ECLIPSE 2100
Data sourced from openFDA. This site is unofficial and independent of the FDA.