The following data is part of a premarket notification filed by Hepatiq Llc with the FDA for Hepatiq.
Device ID | K142891 |
510k Number | K142891 |
Device Name: | HEPATIQ |
Classification | System, Image Processing, Radiological |
Applicant | HEPATIQ LLC 1150 Main Street, Suite E Irvine, CA 92614 |
Contact | Dipu Ghosh |
Correspondent | Dipu Ghosh HEPATIQ LLC 1150 Main Street, Suite E Irvine, CA 92614 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-10-03 |
Decision Date | 2014-12-17 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HEPATIQ 90240856 not registered Live/Pending |
HEPATIQ, INC. 2020-10-07 |
HEPATIQ 86192070 4810355 Live/Registered |
HEPATIQ, INC. 2014-02-12 |