ClearanceBrief
Company ยท US

Rocky Mountain Research, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1992 to 1999. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FIGClamp, Tubing, Blood, Automatic2
KRLDetector, Bubble, Cardiopulmonary Bypass2
DTWMonitor And/Or Control, Level Sensing, Cardiopulmonary Bypass1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 10, 1999K992857LEVELSENS - FLEXIBLE, MODEL 201110, LEVELSENS - RIGID, MODEL 201070
Rocky Mountain Research, Inc.
DTW
Oct 31, 1996K961364AUTOMATIC TUBING CLAMP SYSTEM (ATC)
Rocky Mountain Research, Inc.
KRL
Oct 29, 1996K961598ELS AUTOMATIC TUBING CLAMP SYSTEM
Rocky Mountain Research, Inc.
KRL
Jan 5, 1994K921993ELS AUTOMATIC TUBING CLAMP SYSTEM
Rocky Mountain Research, Inc.
FIG
Jun 24, 1992K914459AUTOMATIC TUBING CLAMP
Rocky Mountain Research, Inc.
FIG

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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