Medical Device Recalls
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1 result found
510(K) Number: K123556 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Mortara Surveyor S12 and Surveyor S19 Patient Monitors. Product Usage: They are indicated for us... | 2 | 10/22/2014 |
FEI # 2183461 Mortara Instrument, Inc |
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