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 |