Medical Device Recalls
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1 result found
510(K) Number: K042894 |
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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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Imalux Niris OCT Imaging System Probe, Model Number 1300, Serial Number F464019, IMALUX Corporation,... | 3 | 02/01/2012 | Imalux Corporation |
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