Genicon, LC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K030174GENICON LAPAROSCOPESJune 19, 2003
K030269GENICON CLIP APPLIERMarch 20, 2003
K002542REUSABLE CANNULAOctober 23, 2000
K993625INSUFFLATION NEEDLE- 120MM, MODEL 900-200June 20, 2000
K991382SHIELDEDTROCAR/CANNULA SYSTEM, MODEL 101-005-101July 15, 1999
K982472GENICON TROCARFebruary 4, 1999