Dailycare Biomedical, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K172778 | CheckMyHeart Plus | July 5, 2018 |
| K062894 | INSTANTCHECK RTD-ECG MONITOR, MODEL RMH4.0 | February 8, 2007 |
| K052303 | READMYHEART, MODEL RMH2.0 | December 16, 2005 |
| K050620 | READMYHEART, MODEL RMH3.0 | July 14, 2005 |
| K042814 | READMYHEART | January 6, 2005 |