Medical Device Recalls
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1 to 3 of 3 Results
Recall Date to: 12/22/2014 510(K) Number: K030795 |
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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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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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