Memtec Corp.
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) | K103427 | MOBILEECG SYSTEM | DPS | 2011-03-24 | View |
| 510(k) | K102723 | MODEL 950-12L HOLTER RECORDER WITHOUT ANALYSIS | MWJ | 2010-12-09 | View |
| 510(k) | K944180 | MODEL 700 | DSH | 1997-03-07 | View |
No matching devices.
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