Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K070588 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Philips SureSigns VSV (Vital Signs Viewer), 863067 Indicated for central monitoring of multiple a... | 2 | 08/22/2018 | Philips Electronics North America Corporation |
| SureSigns Vital Signs Monitors (VS3)-Vital Signs Viewer Central Viewing Station View up to 12 VM mon... | 2 | 11/23/2009 | Philips Healthcare Inc. |
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