Dailycare Biomedical, Inc.

FDA Regulatory Profile

Dailycare Biomedical, Inc. has 0 FDA recalls, 0 inspections, 5 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Jul 5, 2018

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances5Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K172778CheckMyHeart PlusJul 5, 2018
K062894INSTANTCHECK RTD-ECG MONITOR, MODEL RMH4.0Feb 8, 2007
K052303READMYHEART, MODEL RMH2.0Dec 16, 2005
K050620READMYHEART, MODEL RMH3.0Jul 14, 2005
K042814READMYHEARTJan 6, 2005