# Kestra Medical Technologies, Inc.

- Location (FDA's records): Kirkland
- FDA decisions: 2 (2021–2024): 1 510(k) clearance and 1 original PMA approval
- Product codes: MVK (1), MWJ (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Biotricity: 2 (https://510kreport.com/company/biotricity)

## Recent decisions
- K233864: ASSURE Wearable ECG (May 7, 2024)
- P200037: ASSURE Wearable Cardioverter Defibrillator (WCD) System (Jul 27, 2021)

Source page: https://510kreport.com/company/kestra-medical-technologies