Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K042569 |
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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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| Medrad Veris MR Monitor units The system is intended to monitor physiological parameters of pat... | 2 | 01/23/2014 |
FEI # 3006316319 Medrad Mr Inc |
| DC power cable (p/n 3010556) supplied with the MEDRAD(R) Veris MR Vital Signs Monitor: Product U... | 2 | 06/25/2013 |
FEI # 2520313 Medrad Inc |
| Veris Invasive Blood Pressure Interface Cables-Part # 3010478. The product is an accessory to patie... | 2 | 12/15/2006 |
FEI # 2520313 Medrad Inc |
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