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FDA 510(k) Applications for Medical Device Product Code "LEZ"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K091682 | LSVT GLOBAL, LLC | LSVT C OR LSVT COMPANION, MODEL V.1 | 08/20/2009 |
K982396 | RSQ, LLC. | VISIVOX, MODEL V-2 | 09/14/1998 |