Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K053174 |
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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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Evaluation Kit, LOFLO Engine, Respironics/Philips product. Intended use of the LoFlo C5 CO2 senso... | 2 | 04/08/2010 | Philips Healthcare Inc. |
C5 LOFLO Evaluation Kit, Respironics/Philips product. Intended use of the LoFlo C5 CO2 sensor is ... | 2 | 04/08/2010 | Philips Healthcare Inc. |
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