G-Vitri Vitrification Freeze Media; G-Vitri Vitrification Thawing Media— 510(k) K232942
Substantially EquivalentGimbo Medical Technology Shenzhen Co., Ltd.
FDA 510(k) clearance K232942 for G-Vitri Vitrification Freeze Media; G-Vitri Vitrification Thawing Media, Substantially Equivalent on 2024-01-30. Applicant: Gimbo Medical Technology Shenzhen Co., Ltd..
Clearance details
- Applicant
- Gimbo Medical Technology Shenzhen Co., Ltd.
- Product code
- Code MQL
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen, CN
Data sourced from openFDA. This site is unofficial and independent of the FDA.