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FDA 510(k) Applications for Medical Device Product Code "LZB"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K052387 | ARTHREX, INC. | ARTHREX FINGERSHIELD FINGER GUARD, MODEL AR-7199-XX | 11/29/2005 |
K992539 | DIGIT-PRO | PERCUGUARD | 02/18/2000 |
K980827 | TUCKER & ASSOCIATES | LATEX FINGER COT, POWDER-FREE, WITH PROTEIN LABELING | 05/04/1998 |