Medigroup
Naperville, IL, US
Medigroup appears in FDA device records in Naperville, IL. FDA records list 15 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 15
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 15 510(k) clearances for Medigroup between 1983 and 2012. The busiest year on record is 1983, with 9. The most recent is 2012, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1983 | 9 |
| 1998 | 1 |
| 2003 | 1 |
| 2006 | 1 |
| 2007 | 2 |
| 2012 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K120130 | FALLER TROCAR | FJS | Substantially Equivalent | |
| K071167 | FLEX-NECK EXXTENDED PERITONEAL DIALYSIS CATHETER AND ACCESSORIES, MODEL CF-5560 | FJS | Unknown | |
| K070730 | FLEX-NECK ARC CATHETER | FJS | Unknown | |
| K060897 | EMBEDDING TOOL, MODEL TE-1000 | FJS | Substantially Equivalent | |
| K031351 | FLEX-NECK PD CATHETER, INFANT | FJS | Substantially Equivalent | |
| K974570 | PERITONEAL DIALYSIS CATHETER CONNECTOR | FKO | Substantially Equivalent | |
| K823294 | MEDIGROUP LS-110 LIGHT SOURCE | HET | Substantially Equivalent | |
| K823297 | ST-610 NEEDLESCOPE STERILIZATION TRAY | HET | Substantially Equivalent | |
| K823295 | MEDIGROUP 2.2MM NEEDLESCOPE CANNULA& | HET | Substantially Equivalent | |
| K823293 | MEDIGROUP LG-102 LIGHT GUIDE | HET | Substantially Equivalent | |
| K823390 | PC 201A LOCKING SLEEVE | FKX | Substantially Equivalent | |
| K823331 | PC-204 TUNNELOR | FKX | Substantially Equivalent | |
| K823330 | DIALATORS PC-203 & 202 | FKX | Substantially Equivalent | |
| K823303 | QUILL CATHETER GUIDE | FKX | Substantially Equivalent | |
| K823296 | PC-205 TENCKHOFF CATHETER ROD OBTURATOR | FKX | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain