Medphone Corp.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K911604 | MDPHONE CELLULAR + RESCUE (DEFIB SYSTEM) | LDD | 1991-09-23 | View |
| 510(k) | K864257 | TELEPHONE DEFIBRILLATOR SYSTEM | LDD | 1987-11-27 | View |
No matching devices.
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