Medical Device Recalls
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1 result found
510(K) Number: K963952 |
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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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GE OEC 9600 C-arm Fluoroscopy System, GE Healthcare, Surgery, Salt Lake City, Utah. | 2 | 09/20/2008 | OEC Medical Systems, Inc |
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