K240307
- 510(k) number
- K240307
- Device name
- VitaVitro Embryo Transfer Catheter (Models ET-S, ET-SI, ET-A, ET-I, ET-IH)
- Applicant
- Shenzhen Vitavitro Biotech Co., Ltd. CN
- Product code
- MQF — Catheter, Assisted Reproduction
- Decision date
- 2024-08-16
- Date received
- 2024-02-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K240307.pdf
Official FDA record: K240307
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.