The following data is part of a premarket notification filed by Livemetric (medical) S.a. with the FDA for Liveone.
Device ID | K201302 |
510k Number | K201302 |
Device Name: | LiveOne |
Classification | System, Measurement, Blood-pressure, Non-invasive |
Applicant | LiveMetric (Medical) S.A. 40 Rue Glesener Luxembourg, LU L-1630 |
Contact | Chen Botvin Moshe |
Correspondent | Chen Botvin Moshe LiveMetric (Medical) S.A. 40 Rue Glesener Luxembourg, LU L-1630 |
Product Code | DXN |
CFR Regulation Number | 870.1130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2020-05-15 |
Decision Date | 2022-05-04 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LIVEONE 97097114 not registered Live/Pending |
LiveXLive Media, Inc. 2021-10-28 |
LIVEONE 90516452 not registered Live/Pending |
LiveXLive Media, Inc. 2021-02-07 |
LIVEONE 85060083 4023644 Dead/Cancelled |
LIVEONE, INC. 2010-06-10 |
LIVEONE 76248872 2738049 Dead/Cancelled |
JPMORGAN CHASE & CO. 2001-05-01 |