Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K170023 |
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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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| SPiN Thoracic Navigation System Model: SYS-4000 (SYS-4000D) | 2 | 02/07/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| Veran : Endobronchial Always on Track Models: INS-0392 AOTT 21ga Needle, 12mm L, 1.8mm OD, 5/BX ... | 2 | 09/29/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| Veran : Percutaneous Models: INS-5620 SPiN Perc Biopsy Needle Guide Kit - 20cm, 5/Bx (includes INS... | 2 | 09/29/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| Veran Endobronchial: Models: INS-5925 SPiN Access Catheter® 180 Degree for use w/ Pentax Scopes ... | 2 | 09/29/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| Veran:SPiN Thoracic Navigation System Models: SYS-4230 SPiN Thoracic Navigation System - 230V 50Hz... | 2 | 09/29/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
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