Sydney IVF Blastocyst Cryopreservation Kit, Sydney IVF Blastocyst Thawing Kit

FDA 510(k) K152717 · William A. Cook Australia Pty. , Ltd.

Substantially Equivalent

510(k) numberK152717

Submission

Device name
Sydney IVF Blastocyst Cryopreservation Kit, Sydney IVF Blastocyst Thawing Kit
Applicant
William A. Cook Australia Pty. , Ltd.
Eight Mile Plains, AU
Received
September 21, 2015
Decision date
May 6, 2016
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MQL – Media, Reproductive
Device class
Class II (moderate risk)
Regulation
21 CFR 884.6180
Specialty
Obstetrics/Gynecology

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K250445Fast Warm - NXMQL · Traditional Fujifilm Irvine Scientific09/12/2025SE
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K251305Ultra-Fast Vitri; Ultra-Fast WarmMQL · Traditional Kitazato Corporation08/26/2025SE
K242640FertiCult Flushing medium; FertiCult Flushing medium with phenol red and gentamicinMQL · Traditional Fertipro NV05/30/2025SE
K242561Dewin Reproductive Media (Dewin Vitrification Kit, Dewin Thawing Kit)MQL · Traditional Donnevie Medical Technology (Shanghai) Co. , Ltd.04/10/2025SE
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K242107CaseMONO™ Culture (CMON); CaseMONO™ w/HEPES (WHMO); CaseBioscience® HTF (HTFC)…MQL · Traditional Casebioscience, Inc.03/21/2025SE

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K153290Sydney IVF Follicle Flush Buffer, Sydney IVF Fertilization Medium, Sydney IVF Cleavage…MQL · Special 01/27/2016SE
K151367Sydney IVF HyaluronidaseMQL · Traditional 01/27/2016SE
K152782Sydney Ivf Sperm Medium, Sydney Ivf Sperm Gradient Kit, Sydney Ivf SpermientMQL · Special 12/21/2015SE
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Questions and answers

When was Sydney IVF Blastocyst Cryopreservation Kit, Sydney IVF Blastocyst Thawing Kit cleared by the FDA?

Sydney IVF Blastocyst Cryopreservation Kit, Sydney IVF Blastocyst Thawing Kit (K152717) received a 510(k) decision of Substantially Equivalent on May 6, 2016, 228 days after the submission was received.

What is the product code of K152717?

The FDA product code is MQL – Media, Reproductive, a Class II (moderate risk) device regulated under 21 CFR 884.6180.