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FDA 510(k)

Sydney IVF Blastocyst Cryopreservation Kit, Sydney IVF Blastocyst Thawing Kit

K-Number: K152717 · 2016-05-06

Decision Date2016-05-06
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Sydney IVF Blastocyst Cryopreservation Kit, Sydney IVF Blastocyst Thawing Kit is the device name listed in this FDA 510(k) record. The listed applicant is William A. Cook Australia Pty. , Ltd.. It received FDA 510(k) clearance on 2016-05-06 under 510(k) number K152717. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Sydney IVF Blastocyst Cryopreservation Kit, Sydney IVF Blastocyst Thawing Kit?

Sydney IVF Blastocyst Cryopreservation Kit, Sydney IVF Blastocyst Thawing Kit is a medical device that received FDA 510(k) clearance on 2016-05-06. The listed applicant is William A. Cook Australia Pty. , Ltd.. The 510(k) number is K152717.

When did Sydney IVF Blastocyst Cryopreservation Kit, Sydney IVF Blastocyst Thawing Kit receive FDA 510(k) clearance?

Sydney IVF Blastocyst Cryopreservation Kit, Sydney IVF Blastocyst Thawing Kit received FDA 510(k) clearance on 2016-05-06, under 510(k) number K152717.

Who is the listed applicant for Sydney IVF Blastocyst Cryopreservation Kit, Sydney IVF Blastocyst Thawing Kit?

The FDA 510(k) record lists William A. Cook Australia Pty. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sydney IVF Blastocyst Cryopreservation Kit, Sydney IVF Blastocyst Thawing Kit?

The FDA product code for Sydney IVF Blastocyst Cryopreservation Kit, Sydney IVF Blastocyst Thawing Kit is MQL.

Other records listing William A. Cook Australia Pty. , Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 9 devices →

Related Devices (Code: MQL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.