Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K122036 |
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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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ViSi Mobile Chest Sensor (3 lead-wire ECG, AAMI), Catalog No. 93-10014 The ViSi Mobile Monitoring... | 2 | 07/29/2013 | Sotera Wireless, Inc. |
ViSi Mobile Monitor, Catalog No. 92-10010 The ViSi Mobile Monitoring System is intended for use b... | 2 | 07/29/2013 | Sotera Wireless, Inc. |
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