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FDA 510(k)

MC2 Portable X-ray System

K-Number: K241567 · 2024-12-06

ApplicantOxos Medical
Decision Date2024-12-06
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MC2 Portable X-ray System is the device name listed in this FDA 510(k) record. The listed applicant is Oxos Medical. It received FDA 510(k) clearance on 2024-12-06 under 510(k) number K241567. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MC2 Portable X-ray System?

MC2 Portable X-ray System is a medical device that received FDA 510(k) clearance on 2024-12-06. The listed applicant is Oxos Medical. The 510(k) number is K241567.

When did MC2 Portable X-ray System receive FDA 510(k) clearance?

MC2 Portable X-ray System received FDA 510(k) clearance on 2024-12-06, under 510(k) number K241567.

Who is the listed applicant for MC2 Portable X-ray System?

The FDA 510(k) record lists Oxos Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MC2 Portable X-ray System?

The FDA product code for MC2 Portable X-ray System is OWB.

Other records listing Oxos Medical as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: OWB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.