Company ยท US
Medigroup
FDA 510(k) clearances and medical device recalls filed under this name, 1983 to 2012. Name variants (Inc, Corp, punctuation) are merged.
15510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| May 21, 2012 | K120130 | FALLER TROCAR Medigroup, Inc. | FJS |
| Aug 31, 2007 | K071167 | FLEX-NECK EXXTENDED PERITONEAL DIALYSIS CATHETER AND ACCESSORIES, MODEL CF-5560 Medigroup, Inc. | FJS |
| Jul 3, 2007 | K070730 | FLEX-NECK ARC CATHETER Medigroup, Inc. | FJS |
| Jul 18, 2006 | K060897 | EMBEDDING TOOL, MODEL TE-1000 Medigroup, Inc. | FJS |
| Sep 17, 2003 | K031351 | FLEX-NECK PD CATHETER, INFANT Medigroup, Inc. | FJS |
| Feb 27, 1998 | K974570 | PERITONEAL DIALYSIS CATHETER CONNECTOR Medigroup, Inc. | FKO |
| May 9, 1983 | K823294 | MEDIGROUP LS-110 LIGHT SOURCE Medigroup | HET |
| May 6, 1983 | K823297 | ST-610 NEEDLESCOPE STERILIZATION TRAY Medigroup | HET |
| May 6, 1983 | K823295 | MEDIGROUP 2.2MM NEEDLESCOPE CANNULA& Medigroup | HET |
| May 5, 1983 | K823293 | MEDIGROUP LG-102 LIGHT GUIDE Medigroup | HET |
| Jan 26, 1983 | K823390 | PC 201A LOCKING SLEEVE Medigroup | FKX |
| Jan 26, 1983 | K823331 | PC-204 TUNNELOR Medigroup | FKX |
| Jan 26, 1983 | K823330 | DIALATORS PC-203 & 202 Medigroup | FKX |
| Jan 26, 1983 | K823303 | QUILL CATHETER GUIDE Medigroup | FKX |
| Jan 26, 1983 | K823296 | PC-205 TENCKHOFF CATHETER ROD OBTURATOR Medigroup | FKX |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||