VITRIFREEZE MEDIUM; VITRITHAW MEDIUM— 510(k) K070135

Name: FDA 510(k) clearance K070135
Creator: U.S. Food and Drug Administration
Published: 2007-08-16

Substantially Equivalent

Fertipro NV

FDA 510(k) clearance K070135 for VITRIFREEZE MEDIUM; VITRITHAW MEDIUM, Substantially Equivalent on 2007-08-16. Applicant: Fertipro NV. Device class: 2.

Clearance details

Applicant: Fertipro NV
Product code: Code MQL
Device class: Class 2
Regulation: 21 CFR 884.6180
Advisory panel: Obstetrics/Gynecology
Date received: 2007-01-16
Decision date: 2007-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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