RAPID-I— 510(k) K090832

Substantially Equivalent

Vitrolife Sweden AB

FDA 510(k) clearance K090832 for RAPID-I, Substantially Equivalent on 2009-12-23. Applicant: Vitrolife Sweden AB.

Clearance details

Applicant: Vitrolife Sweden AB
Product code: Code MQK
Advisory panel: Obstetrics/Gynecology
Date received: 2009-03-26
Decision date: 2009-12-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Se-400 92 Goteborg, SE

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