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Monarch Platform, Urology

K213334 Class II Traditional
Decision Date
2022-04-29
Sponsor / Applicant
Auris Health, Inc.

Technical Specification

510(k) Submission ID K213334
Product Code FGB
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2022-04-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Monarch Platform, Urology received FDA 510(k) clearance under submission number K213334, sponsored by Auris Health, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2022-04-29.

Classification & Regulation

This clearance is catalogued under FDA product code FGB and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.