Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K120151 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ConMed 50L abdominal insufflator, Catalog Number 72-00258-0 / GS2000 - Product Usage: The device wil... | 2 | 02/24/2021 |
FEI # 1450997 Northgate Technologies, Inc. |
| Insufflator, laparoscopic The ConMed GS2000, Smith & Nephew 500, Novadaq 50L and Nebulae I insuff... | 2 | 12/21/2016 |
FEI # 1450997 Northgate Technologies, Inc. |
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