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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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