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FDA 510(k)

RADIOMED MARKER

K-Number: K022326 · 2003-01-31

ApplicantRadiomed Corporation
Decision Date2003-01-31
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RADIOMED MARKER is the device name listed in this FDA 510(k) record. The listed applicant is Radiomed Corporation. It received FDA 510(k) clearance on 2003-01-31 under 510(k) number K022326. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIOMED MARKER?

RADIOMED MARKER is a medical device that received FDA 510(k) clearance on 2003-01-31. The listed applicant is Radiomed Corporation. The 510(k) number is K022326.

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

RADIOMED MARKER received FDA 510(k) clearance on 2003-01-31, under 510(k) number K022326.

Who is the listed applicant for RADIOMED MARKER?

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

What is the FDA product code for RADIOMED MARKER?

The FDA product code for RADIOMED MARKER is JAK.

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Other records listing Radiomed Corporation 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.

K161724Visicoil MR Marker (User Loaded), Visicoil MR Marker (Pre-Loaded)K120859PRE-LOADED GOLD VISICOIL CK MARKERK070305PRE-LOADED VISICOILK013660GENETRA

Related Devices (Code: JAK)

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.

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Official Source

View on FDA Database →

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

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