LIFEVEST WEARABLE DEFIBRILLATOR
FDA premarket approval P010030/S090 · decided 2017-08-29
Approval details
- PMA number
- P010030
- Supplement
- S090
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- LIFEVEST WEARABLE DEFIBRILLATOR
- Generic name
- Wearable automated external defibrillator
- Applicant
- Zoll Manufacturing Corporation
- Date received
- 2017-01-05
- Decision date
- 2017-08-29
- Days to decision
- 236 days
- Decision code
- APPR
- Product code
- MVK
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Pittsburgh, PA
- Statement
- Approval for new software version (V07.7M) for the LifeVest WCD 4000 Monitor; new software version (V07.2C3) for the LifeVest WCD 4000 Charger; and hardware changes to the LCD display flex tail used in both the WCD 4000 Monitor and WCD 4000 Charger.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| ZOLL Arrhythmia Management Sysyem (K190939) | Zoll Manufacturing Corporation | 2019-12-19 |
| ZOLL ECG Analysis Software (K182093) | Zoll Manufacturing Corporation | 2019-01-28 |
| µCor Heart Failure and Arrhythmia Management System (K172510) | Zoll Manufacturing Corporation | 2018-05-11 |