Medical Device Recalls
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1 result found
510(K) Number: K964414 |
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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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SCOPIX ® LR 5200P® Laser Imagers, Type 8394/600, serial numbers between 4000 and 5266. | 2 | 12/11/2003 | AGFA Corp. |
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