EmbryoScope+— 510(k) K173264

Substantially Equivalent

Vitrolife A/S

FDA 510(k) clearance K173264 for EmbryoScope+, Substantially Equivalent on 2018-05-11. Applicant: Vitrolife A/S.

Clearance details

Applicant: Vitrolife A/S
Product code: Code MQG
Advisory panel: Obstetrics/Gynecology
Date received: 2017-10-11
Decision date: 2018-05-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Viby J, DK

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