Medical Device Recalls
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1 result found
510(K) Number: K830228 |
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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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Armstrong Grommet with wire Otological Ventilation Tube Catalog #: VT-0507-01, Sterilized by Ethyl... | 2 | 06/09/2014 | Summit Medical, Inc. |
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