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 |