The following data is part of a premarket notification filed by Peridot Technologies Ny Inc with the FDA for Sonovision.
| Device ID | K113082 |
| 510k Number | K113082 |
| Device Name: | SONOVISION |
| Classification | System, Image Processing, Radiological |
| Applicant | PERIDOT TECHNOLOGIES NY INC 9131 QUEENS BLVD. SUITE U Elmhurst, NY 11373 |
| Contact | Omar Barlas |
| Correspondent | Omar Barlas PERIDOT TECHNOLOGIES NY INC 9131 QUEENS BLVD. SUITE U Elmhurst, NY 11373 |
| Product Code | LLZ |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-10-18 |
| Decision Date | 2012-03-08 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SONOVISION 90870796 not registered Live/Pending |
Tissue Differentiation Intelligence, LLC 2021-08-07 |
![]() SONOVISION 88243428 not registered Live/Pending |
Tissue Differentiation Intelligence, LLC. 2018-12-27 |
![]() SONOVISION 85828735 4476122 Live/Registered |
Flight Test Aerospace, Inc. 2013-01-22 |
![]() SONOVISION 79272756 not registered Live/Pending |
SONOVISION 2019-06-07 |
![]() SONOVISION 78483361 not registered Dead/Abandoned |
Zubr Comm., LLC 2004-09-14 |
![]() SONOVISION 77122350 not registered Dead/Abandoned |
Stork Vision Brand LLC 2007-03-05 |
![]() SONOVISION 73437800 1343886 Dead/Cancelled |
Cochlea Corp. 1983-08-04 |