Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K110218 |
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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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| Inspira AIR Balloon Dilation System, size 18 x 40; Manufactured by Acclarent, Inc. 1525-G O'Brien... | 1 | 03/01/2012 |
FEI # 3005172759 Acclarent, Inc. |
| INSPIRA AIR BALLOON DILATION SYSTEM 10x40, 1 PK. Airway balloon dilation catheter. | 2 | 05/06/2025 |
FEI # 3003418325 Integra LifeSciences Corp. (NeuroSciences) |
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