MQF
- Product code
- MQF
- Device name
- Catheter, Assisted Reproduction
- Device class
- Class 2
- 21 CFR
- 21 CFR 884.6110
- Medical specialty
- Obstetrics/Gynecology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 4
- Summaries archived here
- 4 (direct download)
- 510(k) clearances (all years, FDA)
- 53 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (4)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K253354 | 2026-02-12 | Guangzhou Hehong Biotech Co., Ltd. | Minvitro Embryo Transfer Catheters (ETCA23175, ETCA2… | |
| K243373 | 2025-07-23 | Vitrolife Sweden AB | Embryo Transfer Catheter (ETC) Assortment: EmbryoCat… | |
| K240307 | 2024-08-16 | Shenzhen Vitavitro Biotech Co., Ltd. | VitaVitro Embryo Transfer Catheter (Models ET-S, ET-… | |
| K231730 | 2023-09-22 | Femasys, Inc. | FemaSeed Intratubal Insemination |
Official FDA classification page: MQF
Classification and pathway per current FDA publications. Data from openFDA (CC0).