Medex, Inc.
Hilliard, OH, US
Medex, Inc. appears in FDA device records in Hilliard, OH. FDA records list 20 510(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
- 20
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 20 510(k) clearances for Medex, Inc. between 1985 and 1999. The busiest year on record is 1988, with 4. The most recent is 1999, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1985 | 1 |
| 1986 | 2 |
| 1987 | 1 |
| 1988 | 4 |
| 1990 | 1 |
| 1991 | 3 |
| 1994 | 4 |
| 1995 | 2 |
| 1998 | 1 |
| 1999 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K982640 | MEDEX 3000 SERIES SYRINGE INFUSION PUMP | FRN | Substantially Equivalent - Subject to Tracking Reg. | |
| K982123 | CONTRAST CONTROL DEVICE | FPA | Substantially Equivalent | |
| K951129 | NOVATRANS II | DRS | Substantially Equivalent | |
| K943897 | NU-SITE | FPA | Substantially Equivalent | |
| K944208 | IV ADMINISTRATION SET FPA | FPA | Substantially Equivalent | |
| K942377 | TRANSTAR PRESSURE TRANSDUCER | DPT | Substantially Equivalent | |
| K940896 | MEDFLATOR II(TM) DISPOSABLE INFLATION DEVICE | MAV | Substantially Equivalent | |
| K922323 | MX4042/MC4044 SERIES SIMULCATH(TM) | KXO | Substantially Equivalent | |
| K913498 | MX927 BLOOD TRANSFER DEVICE | FMI | Substantially Equivalent | |
| K912709 | MX 339 TWIN HEMOSTATIC Y CONNECTOR | DTL | Substantially Equivalent | |
| K910227 | MX4043---SERIES, INTRAUTERINE PRESSURE CATHETER | KXO | Substantially Equivalent | |
| K902771 | ARTERIAL BLOOD SAMPLING KIT | DQO | Substantially Equivalent | |
| K883095 | MX860, REUSABLE PRESSURE TRANSDUCER | DRS | Substantially Equivalent | |
| K883094 | MX350 (SERIES) CONTROL SYRINGE | FMF | Substantially Equivalent | |
| K880696 | MX1002 CABLE-CAL TM | DXG | Substantially Equivalent | |
| K874133 | MX710 SERIES VASCULAR ACCESS INFUSION SET | FPA | Substantially Equivalent | |
| K870301 | MX900-DPT, DISPOSABLE PRESSURE TRANSDUCER | DRS | Substantially Equivalent | |
| K860101 | MX4040 INTRAUTERINE PRESSURE MONITORING KIT | KXO | Substantially Equivalent | |
| K853814 | MP0400 ADULT, PERISTALIC INFUSION PUMP | FRN | Substantially Equivalent | |
| K844631 | PERIFLUX PF-2 | DPW | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- DTLAdaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
- DQOCatheter, Intravascular, Diagnostic
- DXGComputer, Diagnostic, Pre-Programmed, Single-Function
- DPWFlowmeter, Blood, Cardiovascular
- KXOMonitor, Pressure, Intrauterine
- FMINeedle, Hypodermic, Single Lumen
- DPTProbe, Blood-Flow, Extravascular
- FRNPump, Infusion
- FPASet, Administration, Intravascular
- MAVSyringe, Balloon Inflation
- FMFSyringe, Piston
- DRSTransducer, Blood-Pressure, Extravascular
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