Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K962928 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Integra Camino Advanced Monitor with Waveform Display Model CAM01 Integra Neurosciences, 311 Enterpr... | 2 | 12/27/2013 | Integra LifeSciences Corp. |
Integra PAC1 Mod 2 Cables used with the Integra MPM, CAM01 Monitors | 3 | 02/03/2012 | Integra LifeSciences Corp |
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