Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K092467 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Brainlab Cranial Navigation System: An Image Guided Surgery System / Stereotactic. Radiology Departm... | 1 | 01/19/2016 |
FEI # 3002619595 Brainlab AG |
| Ultrasound Navigation Software 1.0 and Ultrasound Integration Software for Cranial/ENT Navigation 3.... | 2 | 10/06/2020 |
FEI # 3002619595 Brainlab AG |
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