The Smartpill Corporation
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) | K092342 | SMARTPILL GI MONITORING SYSTEM, VERSION 2.0 | NYV | 2009-10-30 | View |
| 510(k) | K053547 | SMARTPILL GI MONITORING SYSTEM | NYV | 2006-07-18 | View |
No matching devices.
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