Medical Device Recalls
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1 result found
510(K) Number: K951372 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Philips Gallileo Automatic Collimator, Part Numbers: 9896 010 00612, 9896 010 00614, 9896 010 00615.... | 2 | 09/16/2008 |
FEI # 1000524572 Philips Medical Systems North America Co. Phillips |
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