Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K911421 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Superset with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy Port, REF 3521000. Airw... | 2 | 01/08/2020 |
FEI # 1000120301 Intersurgical Inc |
| Superset with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy Port, REF 3503031. Airw... | 2 | 01/08/2020 |
FEI # 1000120301 Intersurgical Inc |
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