Medical Device Recalls
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1 result found
510(K) Number: K980226 |
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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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Angiotech Soft Tissue Biopsy Needle Core: A) Pro-Mag "Short Throw" Biopsy Needle, and Pro-Mag Bi... | 2 | 07/13/2010 | Medical Device Technologies, Inc. |
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