Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K180757 |
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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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D-Clip Standard/Mini Applier, 190mm bayonet, jaw rigid, double action. | 2 | 03/11/2024 | Peter Lazic Gmbh |
D-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action. | 2 | 03/11/2024 | Peter Lazic Gmbh |
D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action. | 2 | 03/11/2024 | Peter Lazic Gmbh |
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