FDA 510(k) Applications for Medical Device Product Code "LZV"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K021502 | ORTHOSONICS, LTD. | OSCAR, MODEL OE3000 | 06/06/2002 |
K961101 | STRYKER CORP. | STRYKER CEMENT REMOVAL SYSTEM | 07/15/1996 |