Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K130368 |
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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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| AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe | 2 | 06/03/2022 |
FEI # 1450997 Northgate Technologies, Inc. |
| Boston Scientific AUTOLITH TOUCH Bipolar Electrohydraulic Lithotripter, REF M005466800. The device ... | 2 | 12/03/2021 |
FEI # 1450997 Northgate Technologies, Inc. |
| Probe, 9 FR AUTOLITH; NTI Catalog Number 9-900-54 - Product Usage: Probes are used for the fragmenta... | 2 | 03/24/2020 |
FEI # 1450997 Northgate Technologies, Inc. |
| AUTOLITH URO-TCH 9FR PROBE 54CM; NTI Catalog Number 9-203-0543 - Product Usage: Probes are used for ... | 2 | 03/24/2020 |
FEI # 1450997 Northgate Technologies, Inc. |
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