The following data is part of a premarket notification filed by Whitecap Technologies Llc with the FDA for Cyma.
Device ID | K150027 |
510k Number | K150027 |
Device Name: | CYMA |
Classification | Powered Laser Surgical Instrument |
Applicant | WhiteCap Technologies LLC 450 W 910S Suite 300 Heber City, UT 84032 |
Contact | Dustin Synider |
Correspondent | Young Chi Bio-Med USA Inc 27 New England Drive Ramsey, NJ 07446 |
Product Code | GEX |
CFR Regulation Number | 878.4810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-01-07 |
Decision Date | 2015-04-03 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CYMA 97612575 not registered Live/Pending |
Chen Yuejia 2022-09-29 |
CYMA 97456999 not registered Live/Pending |
Universal Geneve S.A. 2022-06-14 |
CYMA 90417988 not registered Live/Pending |
Zhao,Shengde 2020-12-28 |
CYMA 88233361 not registered Live/Pending |
Universal Geneve S.A. 2018-12-18 |
CYMA 87728601 5584260 Live/Registered |
CYMA Systems, Inc. 2017-12-20 |
CYMA 86886632 not registered Dead/Abandoned |
CYMA Systems, Inc. 2016-01-26 |
CYMA 86882791 5031482 Live/Registered |
CYMA INTERNATIONAL LTD 2016-01-21 |
CYMA 86870012 5261895 Live/Registered |
Duratech Plastics Corporation 2016-01-08 |
CYMA 86703219 4944941 Live/Registered |
Duratech Plastics Corporation 2015-07-23 |
CYMA 86702859 4962938 Live/Registered |
Duratech Plastics Corporation 2015-07-23 |
CYMA 86491468 5069288 Live/Registered |
CYTEGIC LTD. 2014-12-29 |
CYMA 78787364 3362342 Dead/Cancelled |
Duratech Plastics Corporation 2006-01-09 |