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GLOBALCARDIO

K111320 Class II Traditional
Decision Date
2011-10-07
Sponsor / Applicant
Cardiocomm Solutions, Inc.

Technical Specification

510(k) Submission ID K111320
Product Code DSH
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2800
Decision Date 2011-10-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GLOBALCARDIO received FDA 510(k) clearance under submission number K111320, sponsored by Cardiocomm Solutions, 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 2011-10-07.

Classification & Regulation

This clearance is catalogued under FDA product code DSH and 21 CFR 870.2800, within the Cardiovascular review panel as a Class II device.