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FDA 510(k)

TUCKER EMBRYO CATHETER

K-Number: K023017 · 2002-12-13

Decision Date2002-12-13
Product CodeMQF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TUCKER EMBRYO CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Fertility Technology Resources, Inc.. It received FDA 510(k) clearance on 2002-12-13 under 510(k) number K023017. 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 TUCKER EMBRYO CATHETER?

TUCKER EMBRYO CATHETER is a medical device that received FDA 510(k) clearance on 2002-12-13. The listed applicant is Fertility Technology Resources, Inc.. The 510(k) number is K023017.

When did TUCKER EMBRYO CATHETER receive FDA 510(k) clearance?

TUCKER EMBRYO CATHETER received FDA 510(k) clearance on 2002-12-13, under 510(k) number K023017.

Who is the listed applicant for TUCKER EMBRYO CATHETER?

The FDA 510(k) record lists Fertility Technology Resources, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TUCKER EMBRYO CATHETER?

The FDA product code for TUCKER EMBRYO CATHETER 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.

Other records listing Fertility Technology Resources, Inc. 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.

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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