meddevicedb.com FDA Device Reference

HRVWatch-Mini Wrist Monitor

K201914 Class II Traditional
Decision Date
2021-06-07
Sponsor / Applicant
Taiwan Scientific Corporation

Technical Specification

510(k) Submission ID K201914
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 2021-06-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HRVWatch-Mini Wrist Monitor received FDA 510(k) clearance under submission number K201914, sponsored by Taiwan Scientific Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2021-06-07.

Classification & Regulation

This clearance is catalogued under FDA product code DXN and 21 CFR 870.1130, within the Cardiovascular review panel as a Class II device.