Medical Device Recalls
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1 result found
510(K) Number: K000890 |
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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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Sequoia Oxymatic electronic oxygen conservers. Models OM-302, OM-311 ***and OM-312***. | 2 | 08/03/2005 | Chad Therapeutics Inc |
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