FDA 510(k) Applications Submitted by RadioMed Corporation

FDA 510(k) Number Submission Date Device Name Applicant
K070305 02/01/2007 PRE-LOADED VISICOIL RADIOMED CORPORATION
K120859 03/22/2012 PRE-LOADED GOLD VISICOIL CK MARKER RADIOMED CORPORATION
K022326 07/18/2002 RADIOMED MARKER RADIOMED CORPORATION
K013660 11/06/2001 GENETRA RADIOMED CORPORATION
K161724 06/22/2016 Visicoil MR Marker (User Loaded), Visicoil MR Marker (Pre-Loaded) RadioMed Corporation


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