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Devices · OXOS Medical, Inc.

Micro C Medical Imaging System, M01

510(k)K212654RadiologyIZL

OXOS Medical, Inc. is listed for Micro C Medical Imaging System, M01 (K212654). The FDA list gives February 4, 2022 as the date of the final decision. The lead panel is Radiology, and the database link on the FDA list is the 510(k) pathway. The primary product code on the FDA list is IZL. openFDA did not return a classification record for that code in this copy of the data. openFDA records this submission’s decision description as “Substantially Equivalent.” This paragraph is assembled only from those public fields. It is not an FDA review, not a determination of safety or effectiveness, and not medical advice. Official record: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm?ID=K212654

Official FDA database record

Date of final decision
February 4, 2022
Company on the FDA list
OXOS Medical, Inc.
Lead panel
Radiology
Primary product code
IZL
openFDA device name for the code
System, X-Ray, Mobile
Device class
2
Regulation number
892.1720
openFDA decision description
Substantially Equivalent
openFDA decision code
SESE
Statement or summary label
Summary