Medigroup
Medigroup appears in FDA public data with 0 recalls, 15 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 21, 2012.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 15
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K120130 | FALLER TROCAR | May 21, 2012 |
| K071167 | FLEX-NECK EXXTENDED PERITONEAL DIALYSIS CATHETER AND ACCESSORIES, MODEL CF-5560 | August 31, 2007 |
| K070730 | FLEX-NECK ARC CATHETER | July 3, 2007 |
| K060897 | EMBEDDING TOOL, MODEL TE-1000 | July 18, 2006 |
| K031351 | FLEX-NECK PD CATHETER, INFANT | September 17, 2003 |
| K974570 | PERITONEAL DIALYSIS CATHETER CONNECTOR | February 27, 1998 |
| K823294 | MEDIGROUP LS-110 LIGHT SOURCE | May 9, 1983 |
| K823295 | MEDIGROUP 2.2MM NEEDLESCOPE CANNULA& | May 6, 1983 |
| K823297 | ST-610 NEEDLESCOPE STERILIZATION TRAY | May 6, 1983 |
| K823293 | MEDIGROUP LG-102 LIGHT GUIDE | May 5, 1983 |
| K823296 | PC-205 TENCKHOFF CATHETER ROD OBTURATOR | January 26, 1983 |
| K823390 | PC 201A LOCKING SLEEVE | January 26, 1983 |
| K823303 | QUILL CATHETER GUIDE | January 26, 1983 |
| K823331 | PC-204 TUNNELOR | January 26, 1983 |
| K823330 | DIALATORS PC-203 & 202 | January 26, 1983 |