Medical Device Recalls
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1 result found
510(K) Number: K943508 |
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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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Stryker brand Insufflation Tube Set and High Flow Insufflation Tube Set, Model Numbers: 620-0... | 2 | 06/27/2006 | Stryker Endoscopy |
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