FDA 510(k) Applications Submitted by MRI MANUFACTURING AND RESEARCH, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K982970 08/25/1998 MRI'S ALL SILICONE IRRIGATION 3-WAY FOLEY CATHETER MRI MANUFACTURING AND RESEARCH, INC.
K944676 09/22/1994 MRI'S ALL SILICONE FOLEY CATHETER MRI MANUFACTURING AND RESEARCH, INC.
K083685 12/12/2008 ENDOVIVE LOW PROFILE REPLACEMENT GASTROSTOMY TUBE, MODEL 82XX, 8283, 8284, 8285 MRI MANUFACTURING AND RESEARCH, INC.


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