Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K110166 |
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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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| 20 Gauge V-Lance Knife Model/Catalog Number: 8065912001 Software Version: N/A Product Description... | 2 | 05/30/2024 | Alcon Research LLC |
| ClearCut S Safety Sideport Knife 1.0mm Dual Bevel Model/Catalog Number: 8065771540 Software Versio... | 2 | 05/30/2024 | Alcon Research LLC |
| ClearCut S Safety Sideport Knife 1.2mm Dual Bevel Model/Catalog Number: 8065771541 Software Versio... | 2 | 05/30/2024 | Alcon Research LLC |
| ClearCut Sideport Knife Dual Bevel 1.2mm Angled Model/Catalog Number: 8065921541 Software Version:... | 2 | 05/30/2024 | Alcon Research LLC |
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