What is the FDA product code for EMBRYO TRANSFER CATHETER CC GLIDER?

The FDA product code for EMBRYO TRANSFER CATHETER CC GLIDER is MQF.

FDA 510(k)

<GENX> EMBRYO TRANSFER CATHETER CC GLIDER

K-Number: K991266 · 1999-09-09

Applicant<Genx> Intl., Inc.

Decision Date1999-09-09

Product CodeMQF

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

<GENX> EMBRYO TRANSFER CATHETER CC GLIDER is the device name listed in this FDA 510(k) record. The listed applicant is <Genx> Intl., Inc.. It received FDA 510(k) clearance on 1999-09-09 under 510(k) number K991266. 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 <GENX> EMBRYO TRANSFER CATHETER CC GLIDER?

<GENX> EMBRYO TRANSFER CATHETER CC GLIDER is a medical device that received FDA 510(k) clearance on 1999-09-09. The listed applicant is <Genx> Intl., Inc.. The 510(k) number is K991266.

When did <GENX> EMBRYO TRANSFER CATHETER CC GLIDER receive FDA 510(k) clearance?

<GENX> EMBRYO TRANSFER CATHETER CC GLIDER received FDA 510(k) clearance on 1999-09-09, under 510(k) number K991266.

Who is the listed applicant for <GENX> EMBRYO TRANSFER CATHETER CC GLIDER?

The FDA 510(k) record lists <Genx> Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for <GENX> EMBRYO TRANSFER CATHETER CC GLIDER?

The FDA product code for <GENX> EMBRYO TRANSFER CATHETER CC GLIDER is MQF.

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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.