AED 3 Semi-Automatic, AED 3 Fully Automatic
FDA premarket approval P160015/S022 · decided 2025-05-30
Approval details
- PMA number
- P160015
- Supplement
- S022
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- AED 3 Semi-Automatic, AED 3 Fully Automatic
- Generic name
- Automated external defibrillators (non-wearable)
- Applicant
- ZOLL Medical Corporation
- Date received
- 2025-05-08
- Decision date
- 2025-05-30
- Days to decision
- 22 days
- Decision code
- OK30
- Product code
- MKJ
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Chelsmford, MA
- Statement
- approval for the supplier to implement an automated system during manufacturing of the battery PCBA
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| 731 Series Ventilator (K233486) | ZOLL Medical Corporation | 2024-12-13 |
| ZOLL Propaq M (K202375) | ZOLL Medical Corporation | 2021-03-09 |
| ZOLL Propaq M (K180482) | ZOLL Medical Corporation | 2018-11-30 |
| Power Infuser (K172653) | ZOLL Medical Corporation | 2018-07-18 |
| 731 Series Ventilators (K162832) | ZOLL Medical Corporation | 2017-08-02 |
| Model 330 Multifunction Aspirator (K170533) | ZOLL Medical Corporation | 2017-04-18 |
| ZOLL X Series (K142915) | ZOLL Medical Corporation | 2014-12-03 |
| ZOLL X SERIES (K141774) | ZOLL Medical Corporation | 2014-11-19 |