Medical Device Recalls
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1 result found
510(K) Number: K923813 |
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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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| Monitor Ceiling Suspension for Fluoroscopic and Angiographic X-Ray Systems. | 2 | 07/20/2004 |
FEI # 1000524572 Philips Medical Systems Sales & Service Region No. America |
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