Medical Device Recalls
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1 result found
510(K) Number: K093388 |
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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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Oridion CO2 sampling lines and water traps under the label: Omnistream CO2 Sampling Lines: OmniLin... | 2 | 03/29/2012 | Oridion Medical 1987 Ltd. |
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