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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: K072929
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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LimiTorr INS9020 INS-9020 LIMITORR VOLUME LIMITING EVD 20 ML LimiTorr INS9020SP1 INS-9020SP1 LIMITO... 1 05/20/2019 Integra LifeSciences Corp.
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