FDA 510(k) Applications for Medical Device Product Code "MOQ"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K980224 | ALEXANDER MFG. CO. | ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS822 | 04/02/1998 |
K013133 | NORDIX, INC. | NORDIX INC RECHARGEABLE BATTERY PART NUMBER 2116 | 11/13/2001 |
K081713 | VIDACARE CORPORATION | VERTEBRAL ACCESS SYSTEM BY VIDACARE | 11/21/2008 |