Marquette Medical Systems, Inc.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K993008 | QUANTITATIVE SENTINEL SYSTEM | HGM | 1999-12-06 | View |
| 510(k) | K981024 | QT DISPERSION AND T WAVE ANALYSIS PROGRAM (QT GUARD ANALYSIS SYSTEM) | LOS | 1998-10-06 | View |
| 510(k) | K980495 | MUSE CARDIOVASCULAR INFORMATION SYSTEM | LOS | 1998-05-07 | View |
| 510(k) | K980299 | APEX OXIMETER | DQA | 1998-04-24 | View |
| 510(k) | K980582 | MULTI-LINK CABLE AND LEAD WIRE SYSTEMS | DSA | 1998-03-16 | View |
| 510(k) | K973403 | CARDIOSMART ST | LOS | 1998-03-12 | View |
| 510(k) | K974199 | ACUTE CARDIAC ISCHEMIA TIME-INSENSITIVE PREDICTIVE INSTRUMENT (ACI-TIPI) OPTION | LOS | 1998-02-06 | View |
| 510(k) | K973984 | RAC 2A MODULE HOUSING | CCK | 1998-01-16 | View |
| 510(k) | K970545 | DASH 1000 PATIENT MONITOR | DSI | 1997-05-08 | View |
No matching devices.
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