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FDA 510(k)

INTRAUTERINE INSEMINATION (IUI) CATHETER

K-Number: K092579 · 2010-04-02

ApplicantFertiligent, Ltd.
Decision Date2010-04-02
Product CodeMQF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

INTRAUTERINE INSEMINATION (IUI) CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Fertiligent, Ltd.. It received FDA 510(k) clearance on 2010-04-02 under 510(k) number K092579. 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 INTRAUTERINE INSEMINATION (IUI) CATHETER?

INTRAUTERINE INSEMINATION (IUI) CATHETER is a medical device that received FDA 510(k) clearance on 2010-04-02. The listed applicant is Fertiligent, Ltd.. The 510(k) number is K092579.

When did INTRAUTERINE INSEMINATION (IUI) CATHETER receive FDA 510(k) clearance?

INTRAUTERINE INSEMINATION (IUI) CATHETER received FDA 510(k) clearance on 2010-04-02, under 510(k) number K092579.

Who is the listed applicant for INTRAUTERINE INSEMINATION (IUI) CATHETER?

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

What is the FDA product code for INTRAUTERINE INSEMINATION (IUI) CATHETER?

The FDA product code for INTRAUTERINE INSEMINATION (IUI) CATHETER is MQF.

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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.

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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.

K253354Minvitro Embryo Transfer Catheters (ETCA23175, ETCA23175-C, ETCB20175, ETCB20175-C, ETCB20175-ET, ETCB20175-ET-C)Guangzhou Hehong Biotech Co., Ltd.K243373Embryo Transfer Catheter (ETC) Assortment: EmbryoCath Embryo Transfer Catheter - Pre-curved 230 mm (REF 17500); EmbryoCath Embryo Transfer Catheter - Straight Malleable 180 mm (REF 17501); EmbryoCath Embryo Transfer Catheter - Straight Malleable 230 mm (REF 17502); EmbryoCath Stylet - 180 mm (REF 17510); EmbryoCath Stylet - 230 mm (REF 17511)Vitrolife Sweden ABK240307VitaVitro Embryo Transfer Catheter (Models ET-S, ET-SI, ET-A, ET-I, ET-IH)Shenzhen Vitavitro Biotech Co., Ltd.K231730FemaSeed Intratubal InseminationFemasys, Inc.K220010Daylily Single Use Sterile Embryo Transfer CatheterShanghai Horizon Medical Technology Co., Ltd.K200248Allwin Embryo Transfer Catheters (ETC), Allwin ETC Stylets and Soft ObturatorsAllwin Medical Devices, Inc.

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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