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 |