The following data is part of a premarket notification filed by Rocky Mountain Research, Inc. with the FDA for Automatic Tubing Clamp.
| Device ID | K914459 |
| 510k Number | K914459 |
| Device Name: | AUTOMATIC TUBING CLAMP |
| Classification | Clamp, Tubing, Blood, Automatic |
| Applicant | ROCKY MOUNTAIN RESEARCH, INC. 2715 EAST 3300 SOUTH Salt Lake City, UT 84109 |
| Contact | Therese Davy |
| Correspondent | Therese Davy ROCKY MOUNTAIN RESEARCH, INC. 2715 EAST 3300 SOUTH Salt Lake City, UT 84109 |
| Product Code | FIG |
| CFR Regulation Number | 876.5820 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-10-07 |
| Decision Date | 1992-06-24 |