meddevicedb.com FDA Device Reference

Telemetry Transmitter

K161056 Class II Traditional
Decision Date
2017-02-03
Sponsor / Applicant
Edan Instruments, Inc.

Technical Specification

510(k) Submission ID K161056
Product Code MHX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 2017-02-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Telemetry Transmitter received FDA 510(k) clearance under submission number K161056, sponsored by Edan Instruments, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2017-02-03.

Classification & Regulation

This clearance is catalogued under FDA product code MHX and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.