meddevicedb.com FDA Device Reference

Quantum Pump Console

K173834 Class II Traditional
Decision Date
2018-05-25
Sponsor / Applicant
Spectrum Medical , Ltd.

Technical Specification

510(k) Submission ID K173834
Product Code DTQ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4220
Decision Date 2018-05-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Quantum Pump Console received FDA 510(k) clearance under submission number K173834, sponsored by Spectrum Medical , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2018-05-25.

Classification & Regulation

This clearance is catalogued under FDA product code DTQ and 21 CFR 870.4220, within the Cardiovascular review panel as a Class II device.