FDA 510(k) Applications for Medical Device Product Code "GET"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K960473 | AESCULAP, INC. | AESCULAP POWER SYSTEM HANDPIECE | 03/07/1996 |
K955174 | SODEM DIFFUSION SA | SODEM HIGH SPEED SYSTEM FOR NEUROSURGERY & MEDIAN STYERNOTOMY | 01/22/1996 |