G-Vitri™ Vitrification Straw— 510(k) K240002

Substantially Equivalent

Gimbo 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..

Clearance details

Applicant
Gimbo Medical Technology Shenzhen Co., Ltd.
Product code
Code MQK
Advisory panel
Obstetrics/Gynecology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Shenzhen, CN
Download summary PDFView on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.