K242684 is an FDA 510(k) clearance for the Harioculture TL-16 Time-lapse Incubator. This device is classified as a Accessory, Assisted Reproduction (Class II - Special Controls, product code MQG).
Submitted by Hua Yue Medical Technology Co., Ltd. (Guangzhou, CN). The FDA issued a Cleared decision on May 22, 2025, 258 days after receiving the submission on September 6, 2024.
This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.6120.
| 510(k) Number | K242684 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 06, 2024 |
| Decision Date | May 22, 2025 |
| Days to Decision | 258 days |
| Submission Type | Traditional |
| Review Panel | Obstetrics & Gynecology (OB) |
| Summary | Summary PDF |
| Product Code | MQG - Accessory, Assisted Reproduction |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 884.6120 |