Rocky Mountain Research, Inc. is one of 15134 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rocky Mountain Research, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LEVELSENS - FLEXIBLE, MODEL 201110, LEVELSENS - RIGID, MODEL 201070, AUTOMATIC TUBING CLAMP SYSTEM (ATC), ELS AUTOMATIC TUBING CLAMP SYSTEM
5
Total
5
Cleared
0
Denied
Rocky Mountain Research, Inc. has 5 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 5 cleared submissions from 1992 to 1999. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Rocky Mountain Research, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rocky Mountain Research, Inc.
5 devices
Cleared
Nov 10, 1999
LEVELSENS - FLEXIBLE, MODEL 201110, LEVELSENS - RIGID, MODEL 201070
Cardiovascular
77d
Cleared
Oct 31, 1996
AUTOMATIC TUBING CLAMP SYSTEM (ATC)
Cardiovascular
205d
Cleared
Oct 29, 1996
ELS AUTOMATIC TUBING CLAMP SYSTEM
Cardiovascular
203d
Cleared
Jan 05, 1994
ELS AUTOMATIC TUBING CLAMP SYSTEM
Gastroenterology & Urology
617d
Cleared
Jun 24, 1992
AUTOMATIC TUBING CLAMP
Gastroenterology & Urology
261d