Mri Manufacturing and Research, Inc. is one of 15069 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mri Manufacturing and Research, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ENDOVIVE LOW PROFILE REPLACEMENT GASTROSTOMY TUBE, MODEL 82XX, 8283, 8284, 8285, MRI'S ALL SILICONE IRRIGATION 3-WAY FOLEY CATHETER, MRI'S ALL SILICONE FOLEY CATHETER
3
Total
3
Cleared
0
Denied
Mri Manufacturing and Research, Inc. has 3 FDA 510(k) cleared medical devices. Based in Tucson, US.
Historical record: 3 cleared submissions from 1996 to 2009. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Mri Manufacturing and Research, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Mri Manufacturing and Research, Inc.
3 devices
Cleared
Jun 25, 2009
ENDOVIVE LOW PROFILE REPLACEMENT GASTROSTOMY TUBE, MODEL 82XX, 8283, 8284, 8285
Gastroenterology & Urology
195d
Cleared
Oct 28, 1998
MRI'S ALL SILICONE IRRIGATION 3-WAY FOLEY CATHETER
Gastroenterology & Urology
64d
Cleared
Apr 05, 1996
MRI'S ALL SILICONE FOLEY CATHETER
Gastroenterology & Urology
561d