meddevicedb.com FDA Device Reference

MODEL TT-185 TELEMETRY TRANSMITTER

K851624 Class II Traditional
Decision Date
1986-01-14
Sponsor / Applicant
Eaton Medical Group

Technical Specification

510(k) Submission ID K851624
Product Code DXH
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2920
Decision Date 1986-01-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL TT-185 TELEMETRY TRANSMITTER received FDA 510(k) clearance under submission number K851624, sponsored by Eaton Medical Group. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1986-01-14.

Classification & Regulation

This clearance is catalogued under FDA product code DXH and 21 CFR 870.2920, within the Cardiovascular review panel as a Class II device.