G-FREEZEKIT BLAST — Vitrolife AB (510(k) K032154)

Name: G-FREEZEKIT BLAST — Vitrolife AB (510(k) K032154)
Creator: DeviceClear

G-FREEZEKIT BLAST — Vitrolife AB (510(k) K032154) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: G-FREEZEKIT BLAST; Applicant: Vitrolife AB; Clearance track: 510(k).

Device name	G-FREEZEKIT BLAST
Applicant	Vitrolife AB
Clearance track	510(k)
Submission number	K032154
Decision	Substantially Equivalent
Decision date	2004-05-07
Date received	2003-07-14
Product code	MQL
Device class	2
Medical specialty	Obstetrics/Gynecology
Applicant location	DC, US
Source	openFDA device

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$1999/mo

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