# QT Medical, Inc.

- Location (FDA's records): Diamond Bar, CA
- FDA decisions: 5 (2018–2026): 5 510(k) clearances
- Product codes: DXH (3), DSA (1), DPS (1)
- 510(k) review time since 2016: median 219 days, against 211 for FDA's reviews in the same codes and years (2 of 4 faster)
- Predicates its devices cite: 5 (2 its own); citations of its devices by later devices: 2 (2 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
- Shl Telemedicine International, Ltd.: 1 (https://510kreport.com/company/shl-telemedicine-international)
- Shenzhen Med-Link Electronics Tech Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-med-link-electronics-tech)
- Mortara Instrument, Inc.: 1 (https://510kreport.com/company/mortara-instrument)

## Its most-cited devices
- K180157: QT ECG (2018), cited by 1
- K220795: QT ECG (2022), cited by 1

## Recent decisions
- K260250: QCA 10 Electrocardiograph (QCARD-10); QCA 10W Electrocardiograph (QCARD-10W) (Sep 29, 2026)
- K233521: QT Ecg (QTERD100) (Dec 6, 2023)
- K220795: QT ECG (Sep 26, 2022)
- K200722: PCA-C1 series Patient Cable (Jun 3, 2021)
- K180157: QT ECG (May 4, 2018)

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