The following data is part of a premarket notification filed by Clinical Innovations, Llc with the FDA for Clearview Total.
| Device ID | K131781 |
| 510k Number | K131781 |
| Device Name: | CLEARVIEW TOTAL |
| Classification | Cannula, Manipulator/injector, Uterine |
| Applicant | CLINICAL INNOVATIONS, LLC 747 WEST 4170 SOUTH Murray, UT 84123 |
| Contact | Brian Mcroberts |
| Correspondent | Brian Mcroberts CLINICAL INNOVATIONS, LLC 747 WEST 4170 SOUTH Murray, UT 84123 |
| Product Code | LKF |
| CFR Regulation Number | 884.4530 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-06-17 |
| Decision Date | 2014-05-28 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CLEARVIEW TOTAL 85727459 not registered Dead/Abandoned |
Clinical Innovations, LLC 2012-09-12 |