G-PGD— 510(k) K033101

Substantially Equivalent

Vitrolife Sweden AB

FDA 510(k) clearance K033101 for G-PGD, Substantially Equivalent on 2004-05-07. Applicant: Vitrolife Sweden AB.

Clearance details

Applicant: Vitrolife Sweden AB
Product code: Code MQL
Advisory panel: Obstetrics/Gynecology
Date received: 2003-09-29
Decision date: 2004-05-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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