VitaVitro® Single Lumen Oocyte Retrieval Needle (ORNS-17G, ORNS-18G), VitaVitro® Double Lumen Oocyte Retrieval Needle (ORND-17G)— 510(k) K240523
Substantially EquivalentShenzhen Vitavitro Biotech Co., Ltd.
FDA 510(k) clearance K240523 for VitaVitro® Single Lumen Oocyte Retrieval Needle (ORNS-17G, ORNS-18G), VitaVitro® Double Lumen Oocyte Retrieval Needle (ORND-17G), Substantially Equivalent on 2024-11-15. Applicant: Shenzhen Vitavitro Biotech Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Shenzhen Vitavitro Biotech Co., Ltd.
- Product code
- Code MQE
- Device class
- Class 2
- Regulation
- 21 CFR 884.6100
- 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 allData sourced from openFDA. This site is unofficial and independent of the FDA.