Medical Device Recalls
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1 result found
510(K) Number: K945297 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| InfraVision IR Illuminator Console, model number 220-180-521, manufactured by Stryker Endoscopy San ... | 2 | 01/18/2011 |
FEI # 2936485 Stryker Endoscopy |
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