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Wearable Device, Wearable Package

K191272 Class II Traditional
Decision Date
2019-07-12
Sponsor / Applicant
Current Health , Ltd.

Technical Specification

510(k) Submission ID K191272
Product Code MSX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 2019-07-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Wearable Device, Wearable Package received FDA 510(k) clearance under submission number K191272, sponsored by Current Health , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2019-07-12.

Classification & Regulation

This clearance is catalogued under FDA product code MSX and 21 CFR 870.2300, within the Cardiovascular review panel as a Class II device.