FDA 510(k) Applications Submitted by GENERAL ELECTRIC COMPANY
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K110798 | 03/22/2011 | SENOGRAPHE DS, SENOGRAPHE ESSENTIAL | GENERAL ELECTRIC COMPANY |
| K103485 | 11/26/2010 | SENOGRAPH DS, SENOGRAPH ESSENSTIAL | GENERAL ELECTRIC COMPANY |
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