Medical Device Recalls
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1 result found
510(K) Number: K011016 |
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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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ESD-5, ESD Flexible Endoscopic Suturing Device, Flexible Sew ® Right Device: Flexible TI ® Knot Devi... | 2 | 04/08/2005 | Wilson-Cook Medical Inc |
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