Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K002765 |
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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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| LICOX Complete Brain IMC Probe Kit, Model IM3.ST C | 3 | 03/15/2005 |
FEI # 2023988 Integra Neuro Sciences |
| LICOX CMP Tissue Oxygen Monitor; Catalog numbers REF AC31. Manufacturer GMS Gesellschaft fur medizi... | 2 | 03/03/2011 |
FEI # 3003418325 Integra LifeSciences Corp. |
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