Medical Device Recalls
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1 result found
510(K) Number: K974597 |
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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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ADC Solo & Initia CR 1000, Path Speed CR SP1001, Centricity CR SP1001 and Centricity CR SP 100, imag... | 2 | 01/06/2006 | AGFA Corp. |
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