Core Dynamics, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
23
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K992250CORE AUDIBLE TROCAR IISeptember 24, 1999
K992190CORE POUCHSeptember 1, 1999
K955490LAPAROSCOPIC KNITTERJanuary 22, 1996
K953903LAPAROSCOPIC TROCAR OBTURATOR, 5MM, 10/11MM, 10/12MMOctober 20, 1995
K953409LAPAROSCOPIC TROCAROctober 16, 1995
K950457CANNUAL AND TROCAR, SUPERPUBICMay 5, 1995
K943172CORE DYNAMICS' LAPAROSCOPIC SMOKE ELIMINATORJuly 28, 1994
K935826LAPAROSCOPIC/SUCTION/IRRIGATION PROBEMay 18, 1994
K932118ENDOSCOPIC TRANSMURAL SUTURE NEEDLE SETMarch 17, 1994
K932020ENTREE BLUNT TIP TROCAR AND ADAPTERJanuary 11, 1994
K932021ENTREE CANNULA FASCIA ANCHORSJanuary 11, 1994
K926477BIFURCATED SUCTION/IRRIGAT TUBING SET W/PUSH BUTTONovember 12, 1993
K933909SCOPE WASHOctober 15, 1993
K931138CORE DYNAMICS LAPAROSCIPIC IRRIGATION PUMPSeptember 7, 1993
K932022ENTREE THORACOSCOPY CANNULA SETJuly 28, 1993
K930512SUCTION/IRRIGATION Y TUBING SET W/TRUMPET VALVESJuly 23, 1993
K924410LAPAROSCOPIC/ENDOSCOPIC INSTRUMENTATIONJune 25, 1993
K922655SUCTION/IRRIGATION Y TUBING SETJuly 14, 1992
K914426ENTREE NEEDLENovember 27, 1991
K911813ENTREE CANNULAJuly 19, 1991