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FDA 510(k)

Towako Transmyometrial Embryo Transfer Set

K-Number: K173431 · 2018-05-18

Decision Date2018-05-18
Product CodeMQF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Towako Transmyometrial Embryo Transfer Set 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 2018-05-18 under 510(k) number K173431. The device is classified under product code MQF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Towako Transmyometrial Embryo Transfer Set?

Towako Transmyometrial Embryo Transfer Set is a medical device that received FDA 510(k) clearance on 2018-05-18. The listed applicant is William A. Cook Australia Pty. , Ltd.. The 510(k) number is K173431.

When did Towako Transmyometrial Embryo Transfer Set receive FDA 510(k) clearance?

Towako Transmyometrial Embryo Transfer Set received FDA 510(k) clearance on 2018-05-18, under 510(k) number K173431.

Who is the listed applicant for Towako Transmyometrial Embryo Transfer Set?

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 Towako Transmyometrial Embryo Transfer Set?

The FDA product code for Towako Transmyometrial Embryo Transfer Set is MQF.

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: MQF)

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.