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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K032971
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Product Description
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FDA Recall
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Sharn TidalGuard SP 710V, Respironics/Philips product. Intended use of the monitors is to provide... 2 04/08/2010 Philips Healthcare Inc.
TidalWave SP 710, Respironics/Philips product. Intended use of the monitors is to provide short t... 2 04/08/2010 Philips Healthcare Inc.
Japanese TidalWave SP 710, Respironics/Philips product. Intended use of the monitors is to provid... 2 04/08/2010 Philips Healthcare Inc.
Refurbished Tidal Wave SP 715, Refurbished, Respironics/Philips product. Intended use of the moni... 2 04/08/2010 Philips Healthcare Inc.
Japanese TidalWave SP 715, Respironics/Philips product. Intended use of the monitors is to provid... 2 04/08/2010 Philips Healthcare Inc.
Resp Profile Monitor, 8100 Cosmo+, Refurbished, Respironics/Philips product. Used to provide spir... 2 04/08/2010 Philips Healthcare Inc.
Tidal Wave Sp Model 715, Respironics/Philips product. Intended use of the monitors is to provide ... 2 04/08/2010 Philips Healthcare Inc.
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