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Molecular Flow Simulations

K201435 Class II Traditional
Decision Date
2021-12-03
Sponsor / Applicant
Therataxis, LLC

Technical Specification

510(k) Submission ID K201435
Product Code HAW
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4560
Decision Date 2021-12-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Molecular Flow Simulations received FDA 510(k) clearance under submission number K201435, sponsored by Therataxis, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2021-12-03.

Classification & Regulation

This clearance is catalogued under FDA product code HAW and 21 CFR 882.4560, within the Neurology review panel as a Class II device.