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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K060096
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Product Description
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FDA Recall
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Kii Shielded Bladed trocars (CTB14), Kii Low profile trocars (CTB23), and Kii 5x55mm Optical Z-Thr... 2 06/14/2017 Applied Medical Resources Corp
Applied Medical 15x100 mm Kii Optical Access Systems, Non-Threaded 6/Box, Model C0R36 Product U... 2 08/24/2011 Applied Medical Resources Corp
Applied Medical 15x100 mm Kii Optical Access Systems, Non-Threaded 6/Box, Model C0R37 Product U... 2 08/24/2011 Applied Medical Resources Corp
Applied Medical 15x100 mm Kii Optical Access Systems, Non-Threaded 6/Box, Model C0R38 Product U... 2 08/24/2011 Applied Medical Resources Corp
Applied Medical 15x100 mm Kii Optical Access Systems, Non-Threaded 6/Box, Model C0R39 Product U... 2 08/24/2011 Applied Medical Resources Corp
Applied Medical 15x100mm Kii Optical Access System, Non-Threaded 6/Box, Model Number: C0R36, Labeled... 2 09/18/2009 Applied Medical Resources Corp
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