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QRS-CARD CARDIOLOGY SUITE

K042799 Class II Traditional
Decision Date
2004-10-22
Sponsor / Applicant
Pulse Biomedical, Inc.

Technical Specification

510(k) Submission ID K042799
Product Code DQK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1425
Decision Date 2004-10-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QRS-CARD CARDIOLOGY SUITE received FDA 510(k) clearance under submission number K042799, sponsored by Pulse Biomedical, 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 2004-10-22.

Classification & Regulation

This clearance is catalogued under FDA product code DQK and 21 CFR 870.1425, within the Cardiovascular review panel as a Class II device.