Marquette Electronics, Inc.
FDA 510(k) & PMA Approved Devices — 82 products
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Total Devices82
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K971868 | IMPACT (INFORMING MOBILE PERSONNEL AND CARE TRACKING) PAGER SYSTEM | MSX | 1997-11-13 | View |
| 510(k) | K971683 | WIRELESS LAN (LOCAL AREA NETWORK) - WIRELESS ETHERNET | MSX | 1997-10-22 | View |
| 510(k) | K972199 | SIGNAL-AVERAGED HIGH RESOLUTION P WAVE ANALYSIS | DPS | 1997-09-25 | View |
| 510(k) | K962547 | CARDIOSERV P | DRO | 1997-03-06 | View |
| 510(k) | K963120 | RESPONDER 2500 DEFIBRILLATOR AND CARDIAC CARE SYSTEM | DRO | 1997-02-28 | View |
| 510(k) | K962827 | ALARM DISPLAY UNIT/PAGER-LAN SYSTEM (ADU) | DSI | 1997-02-24 | View |
| 510(k) | K964750 | EAGLE 4000 PATIENT MONITOR | LOS | 1997-02-21 | View |
| 510(k) | K962551 | CARDIOSERV S | LDD | 1996-11-19 | View |
| 510(k) | K960272 | EAGLE 3000/3100 PATIENT MONITOR | MLD | 1996-10-02 | View |
| 510(k) | K960418 | EAGLE PATIENT MONITOR | DSI | 1996-10-02 | View |
| 510(k) | K961139 | EAGLE PATIENT MONITOR MODEL 3000/3100 | DSI | 1996-08-09 | View |
| 510(k) | K961288 | BODYTRODE | DRX | 1996-08-08 | View |
| 510(k) | K954852 | SOLAR 9000 ANESTHESIA INFORMATION MONITOR | DSI | 1996-05-29 | View |
| 510(k) | K951130 | CARDIOSOFT/CARDIOSYS | LOS | 1996-04-04 | View |
| 510(k) | K952474 | EAGLE 3000 PATIENT MONITOR | DRT | 1995-10-19 | View |
| 510(k) | K952101 | MARQUETTE DEFIB ELECTRODES | MKJ | 1995-09-07 | View |
| 510(k) | K935589 | CENTRA HEART STATION | LOS | 1995-08-24 | View |
| 510(k) | K941262 | MARQUETTE DEFIB ELECTRODE | MKJ | 1995-04-20 | View |
| 510(k) | K950581 | SMART ANESTHESIA MULTI-GAS (SAM) MODULE | CCK | 1995-03-29 | View |
| 510(k) | K943977 | SMART ANESTHESIA MULTI-GAS (SAM) MODULE | CCK | 1995-03-23 | View |
No matching devices.
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