G-IVF G5 SERIES— 510(k) K081116

Substantially Equivalent

Vitrolife Sweden AB

FDA 510(k) clearance K081116 for G-IVF G5 SERIES, Substantially Equivalent on 2008-09-02. Applicant: Vitrolife Sweden AB.

Clearance details

Applicant: Vitrolife Sweden AB
Product code: Code MQL
Advisory panel: Obstetrics/Gynecology
Date received: 2008-04-18
Decision date: 2008-09-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kungsbacka, SE

Download summary PDF View on FDA.gov ↗

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