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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
510(K) Number: K980492
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Recall
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ACMI REF E-1F Electrohydraulic Lithotripsy Probe, 1.9 FR x 120CM 2 07/20/2004 ACMI CORPORATION
ACMI REF E-9F Electrohydraulic Lithotripsy Probe, 9 FR x 60CM 2 07/20/2004 ACMI CORPORATION
ACMI REF E-5F Electrohydraulic Lithotripsy Probe, 5FR x 60CM 2 07/20/2004 ACMI CORPORATION
ACMI REF E-3F Electrohydraulic Lithotripsy Probe, 3 FR x 120CM 2 07/20/2004 ACMI CORPORATION
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