Medical Device Recalls
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1 result found
510(K) Number: K913637 |
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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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ECAT Software Versions V7.1.1b, V7.2, V7.2.1, and V7.2.2 used in the following PET (Positron Emissio... | 2 | 03/21/2003 | Cti Pet Systems Inc |
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