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FDA 510(k)

MRI MARKER

K-Number: K131689 · 2013-11-20

Decision Date2013-11-20
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MRI MARKER is the device name listed in this FDA 510(k) record. The listed applicant is C4 Imaging, LLC. It received FDA 510(k) clearance on 2013-11-20 under 510(k) number K131689. The device is classified under product code KXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MRI MARKER?

MRI MARKER is a medical device that received FDA 510(k) clearance on 2013-11-20. The listed applicant is C4 Imaging, LLC. The 510(k) number is K131689.

When did MRI MARKER receive FDA 510(k) clearance?

MRI MARKER received FDA 510(k) clearance on 2013-11-20, under 510(k) number K131689.

Who is the listed applicant for MRI MARKER?

The FDA 510(k) record lists C4 Imaging, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MRI MARKER?

The FDA product code for MRI MARKER is KXK.

Related Clinical Trials

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.

Other records listing C4 Imaging, LLC 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: KXK)

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.

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