Medical Device Recalls
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21 to 22 of 22 Results
510(K) Number: K955084 |
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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| 10.5CM ANGLE ATTACHMENT, BLACK MAX | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| ***REF BLACKMAX-N***Swivel/Angle Motor Assembly***Rx Only***The Anspach Effort, Inc. Intended for ... | 2 | 01/09/2014 |
FEI # 1045834 The Anspach Effort, Inc. |
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