Medical Device Recalls
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1 result found
510(K) Number: K961590 |
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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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***REF C7122***QTY 1***APEX Arthroscopy Tubing Set. Intended for use for joint irrigation and dis... | 2 | 07/10/2013 | Linvatec Corp. dba ConMed Linvatec |
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