Daylily Single Use Sterile Embryo Transfer Catheter— 510(k) K220010
Substantially EquivalentShanghai Horizon Medical Technology Co., Ltd.
FDA 510(k) clearance K220010 for Daylily Single Use Sterile Embryo Transfer Catheter, Substantially Equivalent on 2022-12-16. Applicant: Shanghai Horizon Medical Technology Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Shanghai Horizon Medical Technology Co., Ltd.
- Product code
- Code MQF
- Device class
- Class 2
- Regulation
- 21 CFR 884.6110
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shanghai, CN
Recent devices under product code MQF
view all- K253354 — Minvitro Embryo Transfer Catheters (ETCA23175, ETCA23175-C, ETCB20175, ETCB20175-C, ETCB20175-ET, ETCB20175-ET-C)
- K243373 — Embryo Transfer Catheter (ETC) Assortment: EmbryoCath Embryo Transfer Catheter - Pre-curved 230 mm (REF 17500) +4 more
- K240307 — VitaVitro Embryo Transfer Catheter (Models ET-S, ET-SI, ET-A, ET-I, ET-IH)
- K231730 — FemaSeed Intratubal Insemination
- K200248 — Allwin Embryo Transfer Catheters (ETC), Allwin ETC Stylets and Soft Obturators
Data sourced from openFDA. This site is unofficial and independent of the FDA.