Medical Device Recalls
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1 result found
510(K) Number: K884268 |
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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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Philips, Voxel Q workstations, untilizing AcQSim or AcQPlan software version 4.2, 4.2.1, 4.9, 4.9.1... | 2 | 11/21/2007 | Philips Medical Systems (Cleveland) Inc |
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