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Micro C Medical Imaging System, M01

K212654 Class II Traditional
Decision Date
2022-02-04
Sponsor / Applicant
Oxos Medical, Inc.

Technical Specification

510(k) Submission ID K212654
Product Code IZL
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1720
Decision Date 2022-02-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Micro C Medical Imaging System, M01 received FDA 510(k) clearance under submission number K212654, sponsored by Oxos Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2022-02-04.

Classification & Regulation

This clearance is catalogued under FDA product code IZL and 21 CFR 892.1720, within the Radiology review panel as a Class II device.