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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K050923
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REF IA-2000-S, LightWave Suction Ablator, STERILE, Rx ONLY, MADE IN USA. CONMED LINVATEC, 11311 CON... 2 09/09/2009 FEI # 1017294
Linvatec Corp. dba ConMed Linvatec
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