G-Vitri Vitrification Straw— 510(k) K240002
Substantially EquivalentGimbo Medical Technology Shenzhen Co., Ltd.
FDA 510(k) clearance K240002 for G-Vitri Vitrification Straw, Substantially Equivalent on 2024-06-14. Applicant: Gimbo Medical Technology Shenzhen Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Gimbo Medical Technology Shenzhen Co., Ltd.
- Product code
- Product code MQK
- Device class
- Class 2
- Regulation
- 21 CFR 884.6160
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen, CN
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Data sourced from openFDA. This site is unofficial and independent of the FDA.