Vitavitro Vitrification Kit, Vitavitro Warming Kit, and Vitavitro Straw Set— 510(k) K180073

Name: FDA 510(k) clearance K180073
Creator: U.S. Food and Drug Administration
Published: 2018-08-29

Substantially Equivalent

Shenzhen Vitavitro Bio-Tech Co., Ltd.

FDA 510(k) clearance K180073 for Vitavitro Vitrification Kit, Vitavitro Warming Kit, and Vitavitro Straw Set, Substantially Equivalent on 2018-08-29. Applicant: Shenzhen Vitavitro Bio-Tech Co., Ltd.. Device class: 2.

Clearance details

Applicant: Shenzhen Vitavitro Bio-Tech Co., Ltd.
Product code: Code MQL
Device class: Class 2
Regulation: 21 CFR 884.6180
Advisory panel: Obstetrics/Gynecology
Date received: 2018-01-09
Decision date: 2018-08-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

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