Cardiogenes

20FDA 510(k) medical device clearances.

Top product codes for Cardiogenes

GEX — General, Plastic Surgery20 devices

Recent clearances by Cardiogenes

K961560 — ECLIPSE 2000Code GEX·1997-01-27
K955006 — ECLIPSE 2100Code GEX·1996-01-17
K952755 — POWERSCULPTOR PROBESCode GEX·1995-09-14
K953658 — CORSSFIRE PLUSCode GEX·1995-08-21
K953424 — ECLIPSE 3200Code GEX·1995-08-11
K945126 — ECLIPSE 3200Code GEX·1995-01-18
K944758 — SUNRISE TECHNOLOGIES MODEL 5020 PLDD KITCode GEX·1994-12-27
K944153 — ECLIPSE 3200Code GEX·1994-11-09
K944151 — OPTICAL FIBER FOR ENT APPLICATIONSCode GEX·1994-11-01
K943171 — CROSSFIRE(TM) (705-10650)Code GEX·1994-09-20
K943311 — ECLIPSE 3200Code GEX·1994-07-22
K931305 — ECLIPSE 3200 FOR USE IN UROLOGY APPLICATIONSCode GEX·1994-01-07
K934935 — ECLIPSE LAZERBLADE(TM) FIBEROPTIC DELIVERY SYSTEMCode GEX·1993-11-22
K931101 — ECLIPSE 2100(TM) MODEL 32, MODIFICATIONCode GEX·1993-08-25
K926210 — ECLIPSE 3200Code GEX·1993-07-28
K931306 — ECLIPSE 3200 FOR USE IN ORTHO SURG/ARTH APPL JOINTCode GEX·1993-07-23
K925840 — ECLIPSE 3200Code GEX·1993-06-25
K924943 — ECLIPSE 3200(TM) HO:YAG LASER FOR PERCU DISKETOMYCode GEX·1993-05-17
K924214 — ECLIPSE 2100(TM) MODEL 32Code GEX·1992-11-16
K921038 — ECLIPSE 2100Code GEX·1992-06-04

Data sourced from openFDA. This site is unofficial and independent of the FDA.