Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K131053 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Otologic Curved Micro Product Usage: Pneumatic system | 2 | 05/04/2017 | The Anspach Effort, Inc. |
| ANSPACH, Rx only, Otologic Curved Micro (OCCM) Diamond Ball Burr, 1.5 MM, Part # OCM7-15SD Produ... | 2 | 05/19/2016 | The Anspach Effort, Inc. |
| ANSPACH, Rx only, Otologic Curved Micro (OCCM) Diamond Ball Burr, 2.0 MM, Part # OCM7-2SD Product... | 2 | 05/19/2016 | The Anspach Effort, Inc. |
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