Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K990202 |
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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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Mizuho Sugita Titanium Standard Aneurysm Clip II , Temporary and permanent occlusion of cervical s... | 2 | 11/22/2013 | Mizuho America, Inc. |
Mizuho Sugita Titanium Standard Aneurysm Clip II , Temporary Mini Type No 58 Temporary and perman... | 2 | 11/22/2013 | Mizuho America, Inc. |
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