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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K893643
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Product Description
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Recall
Class
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FDA Recall
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515B Pulse Oximeter - Dixtal owned product. Intended use is to provide continuous, non-invasive m... 2 04/08/2010 Philips Healthcare Inc.
French 100-120V 515B Pulse Oximeter - Dixtal owned product. Intended use is to provide continuous... 2 04/08/2010 Philips Healthcare Inc.
515B Pulse Oximeter, RS232, Refurbished - Dixtal owned product. Intended use is to provide contin... 2 04/08/2010 Philips Healthcare Inc.
Spanish 100-120V 515B Pulse Oximeter - Dixtal owned product. Intended use is to provide continuou... 2 04/08/2010 Philips Healthcare Inc.
515B Pulse Oximeter, Refurbished - Dixtal owned product. Intended use is to provide continuous, n... 2 04/08/2010 Philips Healthcare Inc.
100-120V 515B with RS-232 Pulse Oximeter - Dixtal owned product. Intended use is to provide conti... 2 04/08/2010 Philips Healthcare Inc.
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