Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K072674 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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 |
Laparoscope, general; plastic surgery Used for general, abdominal, gynecological and thoracic min... | 2 | 01/07/2013 | Applied Medical Resources Corp |
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