Medical Device Recalls
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1 result found
510(K) Number: K903625 |
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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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| PD Access Vascular Access Device. Escalon Vascular Access, Inc., 2440 South 179th Street, New Berlin... | 2 | 10/22/2010 |
FEI # 2183477 Escalon Medical Corp |
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