FDA 510(k) Applications for Medical Device Product Code "DTG"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K960849 | CARDIAC ASSIST DEVICES, INC. | MAGNO ALARM | 03/26/1997 |
K092364 | CYBERONICS, INC. | MODEL 220 PATIENT MAGNET | 11/03/2009 |