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Quantum Ventilation Module

K202733 Class II Special
Decision Date
2020-10-16
Sponsor / Applicant
Spectrum Medical , Ltd.

Technical Specification

510(k) Submission ID K202733
Product Code DTX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4300
Decision Date 2020-10-16
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Quantum Ventilation Module received FDA 510(k) clearance under submission number K202733, sponsored by Spectrum Medical , Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2020-10-16.

Classification & Regulation

This clearance is catalogued under FDA product code DTX and 21 CFR 870.4300, within the Cardiovascular review panel as a Class II device.