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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
Recall Date to: 09/01/2015 510(K) Number: K030795
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Product Description
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FDA Recall
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LS-232 Large 12 LeadWear Single Pack - Disposable ECG Monitoring component intended for use as a rad... 2 09/16/2008 Lifesync Corporation
LS-202 Large LeadWear Combo Pack - Disposable ECG Monitoring component intended for use as a radiofr... 2 09/16/2008 Lifesync Corporation
LifeSync ECG System - Disposable leadwear, Ls-222, Ls-223 2 02/27/2007 GMP Companies/Lifesync Corporation
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