Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K052972 |
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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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DATEX-OHMEDA NETWORK AND ICENTRAL '05, SALES REVISION 4.3 ( Datek-Ohmeda Network and iCentral (inclu... | 2 | 08/12/2010 | Ge Healthcare, Llc |
GE Healthcare, S/5 iCentral and iCentral Client, Related to software licenses L-NET05 and L-NETC05,... | 2 | 04/06/2009 | GE Healthcare |
S/5 iCentral, Cardiovascular Monitoring Devices, Versions L-NET03, L-NETC03, L-NET05 and L-NETC05, G... | 2 | 06/24/2008 | GE Healthcare |
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