Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K913516 |
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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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Japanese 100-120V Oxypleth - 520A Pulse Oximeter- Dixtal owned product. Intended use is to provid... | 2 | 04/08/2010 | Philips Healthcare Inc. |
100-120V Oxypleth - 520A Pulse Oximeter - Dixtal owned product. Intended use is to provide contin... | 2 | 04/08/2010 | Philips Healthcare Inc. |
100-120V Oxypleth - 520A Pulse Oximeter, Refurbished - Dixtal owned product. Intended use is to p... | 2 | 04/08/2010 | Philips Healthcare Inc. |
Span 100-120V 520A - OxyPleth Pulse Oximeter - Dixtal owned product. Intended use is to provide ... | 2 | 04/08/2010 | Philips Healthcare Inc. |
Dixtal Novametrix Neonatal/Pediatric SpO2 Sensor, Foam Wrap Style Catalog #: 6480-25. The SpO2 F... | 2 | 06/28/2009 | Dixtal Medical, Inc. |
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