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FDA 510(k)

TAO EMBRYO TRANSFER CATHETER SYSTEM

K-Number: K012220 · 2001-08-27

Decision Date2001-08-27
Product CodeMQF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TAO EMBRYO TRANSFER CATHETER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ttj Biomedical, LLC. It received FDA 510(k) clearance on 2001-08-27 under 510(k) number K012220. 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 TAO EMBRYO TRANSFER CATHETER SYSTEM?

TAO EMBRYO TRANSFER CATHETER SYSTEM is a medical device that received FDA 510(k) clearance on 2001-08-27. The listed applicant is Ttj Biomedical, LLC. The 510(k) number is K012220.

When did TAO EMBRYO TRANSFER CATHETER SYSTEM receive FDA 510(k) clearance?

TAO EMBRYO TRANSFER CATHETER SYSTEM received FDA 510(k) clearance on 2001-08-27, under 510(k) number K012220.

Who is the listed applicant for TAO EMBRYO TRANSFER CATHETER SYSTEM?

The FDA 510(k) record lists Ttj Biomedical, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TAO EMBRYO TRANSFER CATHETER SYSTEM?

The FDA product code for TAO EMBRYO TRANSFER CATHETER SYSTEM is MQF.

Related Clinical Trials

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.

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

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

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