Sotera Wireless, Inc.
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| ViSi Mobile Monitor, Catalog No. 92-10010 The ViSi Mobile Monitoring System is intended fo recall (Z-1817-2013) | Sotera Wireless, Inc. | 2013-07-29 |
| ViSi Mobile Chest Sensor (3 lead-wire ECG, AAMI), Catalog No. 93-10014 The ViSi Mobile Mon recall (Z-1818-2013) | Sotera Wireless, Inc. | 2013-07-29 |
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Every clearance here is in the API, with alerts when new ones post.