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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K920379
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FDA Recall
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Cosmo - Model 7100 SP02 & ETC02 Monitor, Respironics./Philips product. Intended to be used for mo... 2 04/08/2010 Philips Healthcare Inc.
Cosmo Model 7100 SP02 & ETC02 Monitor, Refurbished, Respironics/Philips product. Intended to be u... 2 04/08/2010 Philips Healthcare Inc.
Spanish 100-120V Cosmo - 7100 Capnograp, Respironics/Philips products. Intended to be used for mo... 2 04/08/2010 Philips Healthcare Inc.
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