# Dailycare Biomedical, Inc.

- Location (FDA's records): Chungli, TW
- FDA decisions: 5 (2005–2018): 5 510(k) clearances
- Product codes: DPS (5)
- Predicates its devices cite: 6 (4 its own); citations of its devices by later devices: 12 (4 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)
- H&C Medical Devices Spa: 1 (https://510kreport.com/company/h-c-medical-devices)

## Firms that cite its devices most
- Beijing Choice Electronic Technololgy Co., Ltd.: 1 (https://510kreport.com/company/beijing-choice-electronic-technololgy)
- Viatom Technology Co., Ltd.: 1 (https://510kreport.com/company/viatom-technology)
- Parama-Tech Company., Ltd.: 1 (https://510kreport.com/company/parama-tech)
- Ld Technology, LLC: 1 (https://510kreport.com/company/ld-technology)
- Reka Pte, Ltd.: 1 (https://510kreport.com/company/reka)
- Cardiocomm Solutions, Inc.: 1 (https://510kreport.com/company/cardiocomm-solutions)
- Mitac International Corp.: 1 (https://510kreport.com/company/mitac-international)
- Taiwan Scientific Corporation: 1 (https://510kreport.com/company/taiwan-scientific)

## Its most-cited devices
- K042814: Readmyheart (2005), cited by 5
- K050620: Readmyheart, Model RMH3.0 (2005), cited by 3
- K052303: Readmyheart, Model RMH2.0 (2005), cited by 3
- K062894: Instantcheck RTD-Ecg Monitor, Model RMH4.0 (2007), cited by 1

## Recent decisions
- K172778: CheckMyHeart Plus (Jul 5, 2018)
- K062894: Instantcheck RTD-Ecg Monitor, Model RMH4.0 (Feb 8, 2007)
- K052303: Readmyheart, Model RMH2.0 (Dec 16, 2005)
- K050620: Readmyheart, Model RMH3.0 (Jul 14, 2005)
- K042814: Readmyheart (Jan 6, 2005)

Source page: https://510kreport.com/company/dailycare-biomedical