FDA applicant
Rocky Mountain Research, Inc.
FDA records 5 decisions for Rocky Mountain Research, Inc. (Salt Lake City, UT) from 1992 to 1999: 5 510(k) clearances. Most are in product codes FIG (Clamp, Tubing, Blood, Automatic) and KRL (Detector, Bubble, Cardiopulmonary Bypass). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Rocky Mountain Research, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Rocky Mountain Research, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Rocky Mountain Research, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Rocky”
FDA records each applicant name separately; these may or may not be the same firm.