Medex, Inc.
Dublin, OH, US
Medex, Inc. appears in FDA device records in Dublin, OH. FDA records list 12 510(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
- 12
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 12 510(k) clearances for Medex, Inc. between 1987 and 2005. The busiest year on record is 1996, with 3. The most recent is 2005, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1987 | 1 |
| 1990 | 2 |
| 1991 | 1 |
| 1995 | 1 |
| 1996 | 3 |
| 2000 | 1 |
| 2002 | 1 |
| 2004 | 1 |
| 2005 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K042432 | PHARMGUARD TOOLBOX, MODEL G6000782 | FRN | Substantially Equivalent | |
| K040899 | MEDEX 3000 SERIES MR SYRINGE INFUSION PUMP | FRN | Substantially Equivalent | |
| K020780 | TRANSTAR INTRACRANIAL PRESSURE TRANSDUCER, MODEL MX950ICP | GWM | Substantially Equivalent | |
| K000328 | MEDEX 3000 SERIES MRI COMPATIBLE SYRINGE INFUSION PUMP | FRN | Substantially Equivalent | |
| K961404 | MX960 REUSABLE PRESSURE TRANSDUCER | DRS | Substantially Equivalent | |
| K961527 | MX703 AND MX730 CONTINUOUS FLUSH DEVICES | KRA | Substantially Equivalent | |
| K954970 | STOPCOCK & LUER LOCK PLUG | FMG | Substantially Equivalent | |
| K952160 | INTRAVASCULAR (I-V) ADMININISTRATION SET (DVGENPERS FPA) | FPA | Substantially Equivalent | |
| K910958 | MEDFLATOR INFLATION SYSTEM | MAV | Substantially Equivalent | |
| K904674 | CENTRAL VENOUS PRESSURE MANOMETER | KRK | Substantially Equivalent | |
| K903199 | HOLLOW LUMEN NEEDLE, PART NUMBER: MX920 | DQO | Substantially Equivalent | |
| K872795 | CHANGE IN STERILITY TEST METHOD & TEST LAB. SITE | FPA | 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
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Data as of , FDA export datePage updated Source: openFDA, public domain