Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K040235 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Licox Brain PMO Probe Kit; Ref IP2.P; Multiparameter Monitoring Oxygen + ICP Channel: Contain Prod... | 2 | 10/28/2010 | Integra LifeSciences Corp. |
Integra, Licox Ref 1P2.P; Brain PMO-Probe Kit Rx only; Contains Products: REF 1P2 Bolt kit for 2 ... | 2 | 04/20/2010 | Integra LifeSciences Corp. |
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