Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K953640 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| AMS DURA-II Universal Tips, 2cm, Product Number 72009361, Sterile, American Medical Systems, Inc. Mi... | 2 | 04/03/2007 |
FEI # 1000116179 American Medical Systems |
| AMS DURA-II Distal Tips, 4 cm, Product Number 72009340, Sterile, American Medical Systems, Inc. Minn... | 2 | 04/03/2007 |
FEI # 1000116179 American Medical Systems |
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