Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K090483 |
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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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Philips SureSigns VM1SpO2, C02, Rec, model no. 863266 - Product Usage: The SureSigns VM1 is a patien... | 2 | 06/10/2020 | Philips North America, LLC |
Philips SureSigns VS2 monitor, 863079 863080 863081 863082 863283 863286 The Sure Signs VS2... | 2 | 08/22/2018 | Philips Electronics North America Corporation |
Philips SureSigns VS3 Vital Signs Monitor Models: VS3 863069, 863070, 453564041251, 453564041261, ... | 2 | 06/17/2011 | Philips Healthcare Inc. |
SureSigns Patient Monitors (VM3, VM4. VM6. VM8): VM3 3/5 lead ECG/SPo2, Respiration Bedside P... | 2 | 11/23/2009 | Philips Healthcare Inc. |
SureSigns Vital Signs Viewer (VSV):Spot Check Vital Signs Monitor with NBP (options to include Predi... | 2 | 11/23/2009 | Philips Healthcare Inc. |
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