K242556 is an FDA 510(k) clearance for the JLK-CTP. This device is classified as a System, Image Processing, Radiological (Class II - Special Controls, product code LLZ).
Submitted by JLK, Inc. (Seoul, KR). The FDA issued a Cleared decision on October 16, 2024, 49 days after receiving the submission on August 28, 2024.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.2050.
| 510(k) Number | K242556 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 28, 2024 |
| Decision Date | October 16, 2024 |
| Days to Decision | 49 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | LLZ - System, Image Processing, Radiological |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.2050 |