Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K133658 |
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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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| CDI Blood parameter monitoring system 500 H/SAT, Part No. 145883 Product Usage: The CDI System 5... | 2 | 08/11/2018 |
FEI # 1828100 Terumo Cardiovascular Systems Corporation |
| Monitor with one Blood Parameter Module and one HSat Probe; 500AHCT Monitor with two Blood Paramete... | 2 | 08/11/2018 |
FEI # 1828100 Terumo Cardiovascular Systems Corporation |
| CDI Blood Parameter Monitoring System 500 Cardiopulmonary bypass on-line blood gas monitor Prod... | 2 | 03/25/2016 |
FEI # 1828100 Terumo Cardiovascular Systems Corporation |
| CDI 500 Blood Parameter Monitoring System. Provides continuous, on-line monitoring of the extracorp... | 2 | 09/09/2015 |
FEI # 1828100 Terumo Cardiovascular Systems Corporation |
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