meddevicedb.com FDA Device Reference

TELEMETRY TRANSMITTER, #TLT-3

K802273 Class II Traditional
Decision Date
1980-10-03
Sponsor / Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic

Technical Specification

510(k) Submission ID K802273
Product Code DRG
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2910
Decision Date 1980-10-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TELEMETRY TRANSMITTER, #TLT-3 received FDA 510(k) clearance under submission number K802273, sponsored by Bd Becton Dickinson Vacutainer Systems Preanalytic. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1980-10-03.

Classification & Regulation

This clearance is catalogued under FDA product code DRG and 21 CFR 870.2910, within the Cardiovascular review panel as a Class II device.