Medical Data Electronics
Arleta, CA, US
Medical Data Electronics appears in FDA device records in Arleta, CA. FDA records list 27 510(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
- 27
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 27 510(k) clearances for Medical Data Electronics between 1985 and 2002. The busiest year on record is 1990, with 4. The most recent is 2002, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1985 | 2 |
| 1986 | 1 |
| 1987 | 1 |
| 1988 | 1 |
| 1989 | 2 |
| 1990 | 4 |
| 1991 | 2 |
| 1992 | 1 |
| 1993 | 1 |
| 1994 | 2 |
| 1996 | 1 |
| 1997 | 3 |
| 1998 | 1 |
| 1999 | 2 |
| 2000 | 1 |
| 2001 | 1 |
| 2002 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K014294 | MODIFICATION TO ESCORT II+ 400 SERIES 9ESCORT PRISM) MONITOR, MODELS 20400, 20401, 20403, 20411, 20412, 20413, 20414 | DQA | Substantially Equivalent | |
| K012336 | MODIFICATION TO:ESCORT VISION CENTRAL STATION TELEMETRY SYSTEM, MODEL 20500 | DSI | Substantially Equivalent | |
| K000660 | ESCORT II+ 400 SERIES (ESCORT PRISM), MODEL 20400, 20401, 20403, MONITOR, MODELS 20411, 20412, 20413 | DRO | Substantially Equivalent | |
| K992413 | ESCORT 100/300 SERIES B (ESCORT II) PATIENT MONITOR | DRT | Substantially Equivalent | |
| K992411 | ESCORT II+ 400 SERIES (ESCORT PRISM) MONITOR | DRT | Substantially Equivalent | |
| K982104 | ESCORT-LINK CENTRAL STATION MONITOR MODEL 20500 | MLD | Substantially Equivalent | |
| K970763 | MODULAR TELEMETRY SYSTEM (MTS) OPTION FOR THE MDE ESCORT II MONITOR | DQA | Substantially Equivalent | |
| K970011 | ESCORT II CLINICAL THERMOMETRY MODULE (CTM) | FLL | Substantially Equivalent | |
| K970012 | ESCORT LINK CENTRAL STATION MONITOR | DSI | Substantially Equivalent | |
| K961138 | ESORT II + 400 SERIES MONITOR | DRO | Substantially Equivalent | |
| K943256 | CARDIAC OUTPUT OPTION 39 | DXG | Substantially Equivalent | |
| K930524 | END TIDAL CO2 OPTION B | CCK | Substantially Equivalent | |
| K930004 | ESCORT 100/300 SERIES B PATIENT MONITORS | DRT | Substantially Equivalent | |
| K915153 | ESCORT-LINK ARRHYTHMIA OPTION 23L | DSI | Substantially Equivalent | |
| K914458 | ESCORT 300A SERIES DEFIBRILLATOR/PACER OPTION | LDD | Substantially Equivalent | |
| K911665 | ESCORT 300 SERIES | LDD | Substantially Equivalent | |
| K902254 | ESCORT MODEL 400T TELEMETRY ECG MONITOR | DXH | Substantially Equivalent | |
| K902060 | ESCORT MODEL 300 | DQA | Substantially Equivalent | |
| K901591 | ESCORT-LINK (MODEL E3200) | DXH | Substantially Equivalent | |
| K896958 | ESCORT NON-INVASIVE BLOOD PRESSURE OPTION | DXN | Substantially Equivalent | |
| K892120 | ESCORT PULSE OXIMETRY OPTION | DQA | Substantially Equivalent | |
| K884742 | ESCORT NON-INVASIVE BLOOD PRESSURE OPTION | DXN | Substantially Equivalent | |
| K881986 | ESCORT - PORTABLE PATIENT MONITOR | DXH | Substantially Equivalent | |
| K872291 | ESCORT PORTABLE PATIENT MONITOR | DXO | Substantially Equivalent | |
| K854234 | ESCORT ECG MONITOR SIEMENS SIRECUST 466 | DPS | Substantially Equivalent | |
| K852958 | PACEPAC | DRO | Substantially Equivalent | |
| K842716 | MDE ESCORT 1000 & MDE ESCOR 2000 | DXH | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- CCKAnalyzer, Gas, Carbon-Dioxide, Gaseous-Phase
- DXGComputer, Diagnostic, Pre-Programmed, Single-Function
- FLLContinuous Measurement Thermometer
- LDDDc-Defibrillator, Low-Energy, (Including Paddles)
- DSIDetector And Alarm, Arrhythmia
- DPSElectrocardiograph
- DRTMonitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
- MLDMonitor, St Segment With Alarm
- DQAOximeter
- DROPacemaker, Cardiac, External Transcutaneous (Non-Invasive)
- DXNSystem, Measurement, Blood-Pressure, Non-Invasive
- DXOTransducer, Pressure, Catheter Tip
- DXHTransmitters And Receivers, Electrocardiograph, Telephone
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