Medical Device Recalls
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1 result found
510(K) Number: K991886 |
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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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Pulsiocath PiCCO ProAQT Monitoring Kit, single-use cardiac output (CO) sensor, one unit per plastic ... | 2 | 02/17/2015 | Pulsion Medical Inc |
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