INSTANTCHECK RTD-ECG MONITOR, MODEL RMH4.0— 510(k) K062894

Substantially Equivalent

Dailycare Biomedical, Inc.

FDA 510(k) clearance K062894 for INSTANTCHECK RTD-ECG MONITOR, MODEL RMH4.0, Substantially Equivalent on 2007-02-08. Applicant: Dailycare Biomedical, Inc..

Clearance details

Applicant: Dailycare Biomedical, Inc.
Product code: Code DPS
Advisory panel: Cardiovascular
Date received: 2006-09-27
Decision date: 2007-02-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chungli, TW

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Adverse events under product code DPS

product code DPS

Death: 7
Total: 7

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.