EmbryoSlide+ ic8 dish— 510(k) K213869

Substantially Equivalent

Vitrolife A/S

FDA 510(k) clearance K213869 for EmbryoSlide+ ic8 dish, Substantially Equivalent on 2022-03-11. Applicant: Vitrolife A/S. Device class: 2.

Clearance details

Applicant
Vitrolife A/S
Product code
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
Viby J, DK
Download summary PDFView on FDA.gov ↗

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