FDA 510(k) Applications for Medical Device Product Code "MXF"
(System,Dental,Hydrokinetic,Carries Removal & Cavity Preparation)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K990219 | BIOLASE TECHNOLOGY, INC. | MODIFICATION OF MILLENNIUM | 02/24/1999 |
| K022803 | BIOLASE TECHNOLOGY, INC. | WATERLASE FOR APICOECTOMY | 02/03/2003 |
| K012511 | BIOLASE TECHNOLOGY, INC. | WATERLASE MILLENNIUM | 01/18/2002 |
| K013908 | BIOLASE TECHNOLOGY, INC. | WATERLASE MILLENNIUM | 02/12/2002 |
| K990908 | ENDO TECHNIC CORP. | MILLENNIUM | 05/27/1999 |
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