FDA 510(k) Applications for Medical Device Product Code "NYV"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K053547 | THE SMARTPILL CORPORATION | SMARTPILL GI MONITORING SYSTEM | 07/18/2006 |
K092342 | THE SMARTPILL CORPORATION | SMARTPILL GI MONITORING SYSTEM, VERSION 2.0 | 10/30/2009 |