RAPID-I KIT— 510(k) K140207

Substantially Equivalent

Vitrolife Sweden AB

FDA 510(k) clearance K140207 for RAPID-I KIT, Substantially Equivalent on 2014-12-18. Applicant: Vitrolife Sweden AB.

Clearance details

Applicant: Vitrolife Sweden AB
Product code: Code MQK
Advisory panel: Obstetrics/Gynecology
Date received: 2014-01-28
Decision date: 2014-12-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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