Medical Device Recalls
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1 result found
510(K) Number: K083688 |
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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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Pulmonetic Systems P/N 19189-001 Patient Circuit SPU W/O PEEP 15 FT 5/Pkg. These circuits are inten... | 2 | 08/10/2010 | CareFusion 203, Inc. |
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