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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: K910019
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Recall
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FDA Recall
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100-120V Capnogard 1265, Respironics/Philips product. Intended to be used for monitoring end tida... 2 04/08/2010 FEI # 1218950
Philips Healthcare Inc.
100-120V Capnogard 1265, Refurbished, Respironics/Philips product. Intended to be used for monito... 2 04/08/2010 FEI # 1218950
Philips Healthcare Inc.
Spanish Capnogard 1265, Respironics/Philips product. Intended to be used for monitoring end tidal... 2 04/08/2010 FEI # 1218950
Philips Healthcare Inc.
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