Midwest Analog & Digital, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K850619 | BEDSIDE PATIENT MONITOR W/MODULES | DRT | 1985-06-06 | View |
| 510(k) | K781873 | RECORDER, STRIP CHART WITH PRINTER | DSF | 1979-01-05 | View |
| 510(k) | K780432 | ARRHYTHMIA PROGRAM MODULE | DSI | 1978-05-26 | View |
No matching devices.
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