Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K963327 |
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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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Tidal wave, Model 610, Respironics/Philips product. Intended use of the monitors is to provide sh... | 2 | 04/08/2010 | Philips Healthcare Inc. |
Tidal Wave - 615, Refurbished, Respironics/Philips product. Intended use of the monitors is to pr... | 2 | 04/08/2010 | Philips Healthcare Inc. |
Tidal Wave 610, Refurbished, Respironics/Philips product. Intended use of the monitors is to prov... | 2 | 04/08/2010 | Philips Healthcare Inc. |
Tidal Wave Model 615, Respironics/Philips product. Intended use of the monitors is to provide sho... | 2 | 04/08/2010 | Philips Healthcare Inc. |
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