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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K954015
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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6 Fr Introducer Set, REF 21-2320-24 2 07/20/2004 Deltec, Inc
8.5 Fr Introducer Set, REF 21-2370-24 2 07/20/2004 Deltec, Inc
9 Fr Introducer Set, REF 21-2340-24 2 07/20/2004 Deltec, Inc
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