meddevicedb.com FDA Device Reference

MEDI-TRACE

K811410 Class II Traditional
Decision Date
1981-06-12
Sponsor / Applicant
Graphic Controls Corp.

Technical Specification

510(k) Submission ID K811410
Product Code KRA
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1210
Decision Date 1981-06-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDI-TRACE received FDA 510(k) clearance under submission number K811410, sponsored by Graphic Controls Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1981-06-12.

Classification & Regulation

This clearance is catalogued under FDA product code KRA and 21 CFR 870.1210, within the Cardiovascular review panel as a Class II device.