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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K904987
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BioPince Full Core Biopsy Instrument packed in aTyvek/plastic blister pack which is labeled as prev... 2 07/20/2004 Medical Device Technologies, Inc.
BioPince Ultra Full Core Biopsy Instrument: REF: REF: 360-1080-01, 360-1080-02, 360-1080-03, 360-158... 2 09/20/2024 Argon Medical Devices, Inc
BioPince Full Core Biopsy Instrument 16ga x 15cm.,Use with Optional CO-Axial Needle MCXS1615BP. QTY... 2 06/25/2020 Argon Medical Devices, Inc
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