Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K140808 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Philips Ultrasound, Model Q-Station, with software version 3 or higher, Catalog number: 795088; Part... | 2 | 06/15/2015 | Philips Ultrasound, Inc. |
| Q-Station Quantification Software. Q-Station 3.0 with a2DQ and/or aCMQ Q-Apps are affected. Model: ... | 2 | 12/16/2014 | Philips Ultrasound, Inc. |
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