Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K080067 |
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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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ellex I.Science iTRACK 250A, Canaloplasty Microcatheter Kit, for single use, REF iT-250A, Rx. The f... | 2 | 10/01/2018 | Ellex iScience, Inc. |
iTRACK250A Canaloplasty Microcatheter Kit; Catalogue number: iT-250A; Rx only, sterile. Indicated... | 2 | 09/04/2014 | Ellex iScience, Inc. |
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