meddevicedb.com FDA Device Reference

MICROMED QRS CARD

K903722 Class II Traditional
Decision Date
1990-12-05
Sponsor / Applicant
Nasiff Assoc., Inc.

Technical Specification

510(k) Submission ID K903722
Product Code DPS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2340
Decision Date 1990-12-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICROMED QRS CARD received FDA 510(k) clearance under submission number K903722, sponsored by Nasiff Assoc., 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 1990-12-05.

Classification & Regulation

This clearance is catalogued under FDA product code DPS and 21 CFR 870.2340, within the Cardiovascular review panel as a Class II device.