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ELECTROCARDIOGRAPHIC CABLHS & LEAD WIRE

K771645 Class II Traditional
Decision Date
1977-10-18
Sponsor / Applicant
Tronomed, Inc.

Technical Specification

510(k) Submission ID K771645
Product Code DSA
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2900
Decision Date 1977-10-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTROCARDIOGRAPHIC CABLHS & LEAD WIRE received FDA 510(k) clearance under submission number K771645, sponsored by Tronomed, 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 1977-10-18.

Classification & Regulation

This clearance is catalogued under FDA product code DSA and 21 CFR 870.2900, within the Cardiovascular review panel as a Class II device.