Medical Device Recalls
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1 result found
510(K) Number: K033030 |
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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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Product is a CALYSTO Series IV Physio-monitoring & Information System model # M-S0053. | 2 | 12/23/2005 | Witt Biomedical Corporation |
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