The following data is part of a premarket notification filed by Lazarus, 3d, Inc with the FDA for Pre-sure.
Device ID | K201835 |
510k Number | K201835 |
Device Name: | PRE-SURE |
Classification | System, Image Processing, Radiological |
Applicant | Lazarus, 3D, Inc 3513 NW Mink Pl Corvallis, OR 97330 |
Contact | Smriti Zanevald |
Correspondent | Elisa Maldonado-holmertz Obelix Consulting 12416 Fairfax Ridge Place Austin, TX 78738 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2020-07-02 |
Decision Date | 2021-07-08 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PRE-SURE 98212393 not registered Live/Pending |
Central States Industrial Equipment & Service, Inc. 2023-10-06 |
PRE-SURE 98169457 not registered Live/Pending |
Lake Products Limited 2023-09-07 |
PRE-SURE 90307808 not registered Live/Pending |
LAZARUS 3D 2020-11-09 |
PRE-SURE 79400926 not registered Live/Pending |
LAKE PRODUCTS LIMITED 2024-03-04 |
PRE-SURE 74257390 1756640 Dead/Cancelled |
Accu-Dent 1992-03-20 |