Lifesync Corporation
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| LS-232 Large 12 LeadWear Single Pack - Disposable ECG Monitoring component intended for us recall (Z-1659-2008) | Lifesync Corporation | 2008-09-16 |
| LS-202 Large LeadWear Combo Pack - Disposable ECG Monitoring component intended for use as recall (Z-1660-2008) | Lifesync Corporation | 2008-09-16 |
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Every clearance here is in the API, with alerts when new ones post.