Michigan Instruments, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K073079 | THUMPER, MODEL: 1008 | DRM | 2008-02-14 | View |
| 510(k) | K972525 | THUMPER | DRM | 1997-10-02 | View |
| 510(k) | K962237 | THUMPER CARDIOPULMONARY RESUSCITATOR | DRM | 1996-09-05 | View |
| 510(k) | K895954 | LARYNGOSTAT LARYNGOSCOPE HANDLE | CCW | 1989-10-30 | View |
| 510(k) | K851139 | THUMPER CARDIOPULMONARY RESUSCITATOR 1005 | DRM | 1985-05-15 | View |
| 510(k) | K833879 | CARDIOPULMONARY RESUSCITATOR | DRM | 1983-12-27 | View |
| 510(k) | K811909 | CARDIOPULMUNARY RESUSCITATOR | DRM | 1981-07-16 | View |
No matching devices.
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