Medical Device Recalls
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1 result found
510(K) Number: K992125 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| DICOM Option for the Norland Illuminatus Software Revs 4.2.0 though 4.3.1. Models Norland XR-600, XR... | 2 | 11/18/2011 |
FEI # 1216677 Cooper Surgical, Inc. |
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