Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K890517 |
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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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Transcutaneous C02 & O2 Monitor - 860, Respironics/Philips product. Used for trending O2 and CO2 ... | 2 | 04/08/2010 | Philips Healthcare Inc. |
Transcutaneous C02 & 02 Monitor - 860, Refurbished, Respironics/Philips product. Used for trendin... | 2 | 04/08/2010 | Philips Healthcare Inc. |
Spanish 100-120V TCOM-860, Respironics/Philips product. Used for trending O2 and CO2 tension at t... | 2 | 04/08/2010 | Philips Healthcare Inc. |
French 100-120V 860 TC C02 & 02 Monitor, Respironics/Philips product. Used for trending O2 and CO... | 2 | 04/08/2010 | Philips Healthcare Inc. |
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