# Shenzhen Viatom Technology Co., Ltd.

- Location (FDA's records): Shenzhen, CN
- FDA decisions: 5 (2019–2025): 5 510(k) clearances
- Product codes: DQA (3), DXN (2)
- 510(k) review time since 2016: median 205 days, against 182 for FDA's reviews in the same codes and years (1 of 5 faster)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 2 (1 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
- Omron Healthcare, Inc.: 1 (https://510kreport.com/company/omron-healthcare)
- Shenzhen Aeon Technology Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-aeon-technology)
- Beijing Choice Electronic Technology Co., Ltd.: 1 (https://510kreport.com/company/beijing-choice-electronic-technology)
- Viatom Technology Co., Ltd.: 1 (https://510kreport.com/company/viatom-technology)
- Andon Health Co, Ltd.: 1 (https://510kreport.com/company/andon-health)

## Firms that cite its devices most
- Wesper, Inc.: 1 (https://510kreport.com/company/wesper)

## Its most-cited devices
- K191088: Checkme O2 Pulse Oximeter (2019), cited by 2

## Recent decisions
- K242876: Pulse Oximeter ( PO2, PO2A, PO2B) (Feb 28, 2025)
- K203812: Oxyfit Pulse Oximeter (Nov 8, 2022)
- K193348: Blood Pressure Monitor (Jun 25, 2020)
- K191088: Checkme O2 Pulse Oximeter (Dec 2, 2019)
- K190207: Blood Pressure Monitor (Aug 19, 2019)

Source page: https://510kreport.com/company/shenzhen-viatom-technology