Medigroup, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
15
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K120130FALLER TROCARMay 21, 2012
K071167FLEX-NECK EXXTENDED PERITONEAL DIALYSIS CATHETER AND ACCESSORIES, MODEL CF-5560August 31, 2007
K070730FLEX-NECK ARC CATHETERJuly 3, 2007
K060897EMBEDDING TOOL, MODEL TE-1000July 18, 2006
K031351FLEX-NECK PD CATHETER, INFANTSeptember 17, 2003
K974570PERITONEAL DIALYSIS CATHETER CONNECTORFebruary 27, 1998
K823294MEDIGROUP LS-110 LIGHT SOURCEMay 9, 1983
K823297ST-610 NEEDLESCOPE STERILIZATION TRAYMay 6, 1983
K823295MEDIGROUP 2.2MM NEEDLESCOPE CANNULA&May 6, 1983
K823293MEDIGROUP LG-102 LIGHT GUIDEMay 5, 1983
K823330DIALATORS PC-203 & 202January 26, 1983
K823331PC-204 TUNNELORJanuary 26, 1983
K823303QUILL CATHETER GUIDEJanuary 26, 1983
K823390PC 201A LOCKING SLEEVEJanuary 26, 1983
K823296PC-205 TENCKHOFF CATHETER ROD OBTURATORJanuary 26, 1983