VitaVitro Embryo Transfer Catheter (Models ET-S, ET-SI, ET-A, ET-I, ET-IH)— 510(k) K240307
Substantially EquivalentShenzhen Vitavitro Biotech Co., Ltd.
FDA 510(k) clearance K240307 for VitaVitro Embryo Transfer Catheter (Models ET-S, ET-SI, ET-A, ET-I, ET-IH), Substantially Equivalent on 2024-08-16. Applicant: Shenzhen Vitavitro Biotech Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Shenzhen Vitavitro Biotech 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
- Shenzhen, CN
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More clearances from Shenzhen Vitavitro Biotech Co., Ltd.
view all- K240523 — VitaVitro® Single Lumen Oocyte Retrieval Needle (ORNS-17G, ORNS-18G), VitaVitro® Double Lumen Oocyte Retrieval Needle (ORND-17G)
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- K200408 — VitaVitro® Fertilization Medium, VitaVitro® Gamete Buffer Medium, VitaVitro® Flushing Buffer Medium
- K191063 — 1-Step Culture Medium
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