Zoe Medical Incorporated
4 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| Spacelabs Ultraview DM3 Vital Signs Monitor (all variations -M, -MT, -N, -NT), Model Numbe recall (Z-3098-2024) | Zoe Medical Incorporated | 2024-09-10 |
| Spacelabs Ultraview DM4 Vital Signs Monitor (all variations -M, -N, -MF, -NF, -MW, -NW, -M recall (Z-3099-2024) | Zoe Medical Incorporated | 2024-09-10 |
| Spacelabs Ultraview DM3 Monitor Model Number: 91330-NT The Ultraview DM3 Monitor is indica recall (Z-2380-2012) | Zoe Medical Incorporated | 2012-09-14 |
| The Well@Home Monitor by Patient Care technologies Model 179-2150 Intended to be used as a recall (Z-2166-2010) | Zoe Medical Incorporated | 2010-08-03 |
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Every clearance here is in the API, with alerts when new ones post.