Medical Device Recalls
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1 result found
510(K) Number: K101850 |
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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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Spacelabs BleaseSirius Anesthesia Workstation, BleaseFocus Anesthesia Workstation, and CAS I/II Abso... | 1 | 03/20/2013 | Del Mar Reynolds Medical, Ltd. |
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