Medical Device Manufacturer · US , Salt Lake City , UT

Rocky Mountain Research, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1992
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.

5 devices
1–5 of 5
LEVELSENS - FLEXIBLE, MODEL 201110, LEVELSENS - RIGID, MODEL 201070
K992857 · DTW Monitor And/or Control, Level Sensing, Cardiopulmonary Bypass · Cardiovascular
Nov 1999 77d
AUTOMATIC TUBING CLAMP SYSTEM (ATC)
K961364 · KRL Detector, Bubble, Cardiopulmonary Bypass · Cardiovascular
Oct 1996 205d
ELS AUTOMATIC TUBING CLAMP SYSTEM
K961598 · KRL Detector, Bubble, Cardiopulmonary Bypass · Cardiovascular
Oct 1996 203d
ELS AUTOMATIC TUBING CLAMP SYSTEM
K921993 · FIG Clamp, Tubing, Blood, Automatic · Gastroenterology & Urology
Jan 1994 617d
AUTOMATIC TUBING CLAMP
K914459 · FIG Clamp, Tubing, Blood, Automatic · Gastroenterology & Urology
Jun 1992 261d
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All5 Cardiovascular 3 Gastroenterology & Urology 2