FDA 510(k) Applications Submitted by 3D LINE USA, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K013535 10/23/2001 EVTOOL MODEL # V. 1.0 3D LINE USA, INC.
K001163 04/10/2000 DMLC IV-ERGO 3D LINE USA, INC.
K011255 04/24/2001 3D LINE STEROTACTIC HARDWARE ACCESSORIES 3D LINE USA, INC.
K031281 04/22/2003 ERGO SRS 3D LINE USA, INC.
K031631 05/27/2003 STEREOTACTIC BODY FRAME, MODEL COD. 70-1A 3D LINE USA, INC.
K034051 12/30/2003 DYNATRAC, COD. 50-1A 3D LINE USA, INC.


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