Medical Device Recalls
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1 result found
510(K) Number: K053106 |
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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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Tego Connector, Item No. D1000, NM1000 The Tego® Needle Free Access Device is intended for use as... | 2 | 01/10/2017 | ICU Medical, Inc. |
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