ClariCT.AI
System, Image Processing, Radiological
ClariPI Inc.
The following data is part of a premarket notification filed by Claripi Inc. with the FDA for Clarict.ai.
Pre-market Notification Details
| Device ID | K183460 |
| 510k Number | K183460 |
| Device Name: | ClariCT.AI |
| Classification | System, Image Processing, Radiological |
| Applicant | ClariPI Inc. 3F, 70-15, Ihwajang-gil Seoul, KR 03088 |
| Contact | Hyun-sook Park |
| Correspondent | Carl Alletto OTech Inc 8317 Belew Drive Mckinney, TX 75071 |
| Product Code | LLZ |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-12-13 |
| Decision Date | 2019-06-13 |
NIH GUDID Devices
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 08800046800006 | K183460 | 000 |
Trademark Results [ClariCT.AI]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CLARICT.AI 88550926 not registered Live/Pending |
ClariPI Inc. 2019-07-30 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.