Aframe Digital, Inc.
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) | K122333 | MOBILECARE MONITOR | DRG | 2012-11-19 | View |
| 510(k) | K090138 | MOBILECARE MONITOR, MODEL 2100 | KMI | 2009-04-24 | View |
No matching devices.
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