Rocky Mountain Research, Inc.
Salt Lake City, UT, US
Rocky Mountain Research, Inc. appears in FDA device records in Salt Lake City, UT. FDA records list 5 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 5
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 5 510(k) clearances for Rocky Mountain Research, Inc. between 1992 and 1999. The busiest year on record is 1996, with 2. The most recent is 1999, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1992 | 1 |
| 1994 | 1 |
| 1996 | 2 |
| 1999 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K992857 | LEVELSENS - FLEXIBLE, MODEL 201110, LEVELSENS - RIGID, MODEL 201070 | DTW | Substantially Equivalent | |
| K961364 | AUTOMATIC TUBING CLAMP SYSTEM (ATC) | KRL | Substantially Equivalent | |
| K961598 | ELS AUTOMATIC TUBING CLAMP SYSTEM | KRL | Substantially Equivalent | |
| K921993 | ELS AUTOMATIC TUBING CLAMP SYSTEM | FIG | Substantially Equivalent | |
| K914459 | AUTOMATIC TUBING CLAMP | FIG | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain