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FDA 510(k)

MORTON IUI CATHETERS

K-Number: K041470 · 2004-11-22

Decision Date2004-11-22
Product CodeMQF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MORTON IUI CATHETERS 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 2004-11-22 under 510(k) number K041470. 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 MORTON IUI CATHETERS?

MORTON IUI CATHETERS is a medical device that received FDA 510(k) clearance on 2004-11-22. The listed applicant is Fertility Technology Resources, Inc.. The 510(k) number is K041470.

When did MORTON IUI CATHETERS receive FDA 510(k) clearance?

MORTON IUI CATHETERS received FDA 510(k) clearance on 2004-11-22, under 510(k) number K041470.

Who is the listed applicant for MORTON IUI CATHETERS?

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 MORTON IUI CATHETERS?

The FDA product code for MORTON IUI CATHETERS 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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