K243833 is an FDA 510(k) clearance for the Portable oxygen concentrator (JAY-1000P). This device is classified as a Generator, Oxygen, Portable (Class II - Special Controls, product code CAW).
Submitted by Longfian Scitech Co., Ltd. (Baoding, CN). The FDA issued a Cleared decision on September 29, 2025, 290 days after receiving the submission on December 13, 2024.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5440.
| 510(k) Number | K243833 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 13, 2024 |
| Decision Date | September 29, 2025 |
| Days to Decision | 290 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | Summary PDF |
| Product Code | CAW - Generator, Oxygen, Portable |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.5440 |