Medical Device Recalls
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1 result found
510(K) Number: K964175 |
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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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| Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; Material # E... | 2 | 04/18/2017 |
FEI # 1219930 COVIDIEN MEDTRONIC |
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