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FDA 510(k)

iVitri Straw

K-Number: K172751 · 2018-02-09

ApplicantReprobitech Corp.
Decision Date2018-02-09
Product CodeMQK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

iVitri Straw is a medical device manufactured by Reprobitech Corp.. It received FDA 510(k) clearance on 2018-02-09 under approval number K172751. The device is classified under product code MQK. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the iVitri Straw?

iVitri Straw is a medical device that received FDA 510(k) clearance on 2018-02-09. It is manufactured by Reprobitech Corp.. The 510(k) number is K172751.

When was iVitri Straw approved by the FDA?

iVitri Straw received FDA 510(k) clearance on 2018-02-09, under approval number K172751.

What company makes iVitri Straw?

iVitri Straw is manufactured by Reprobitech Corp..

What is the FDA product code for iVitri Straw?

The FDA product code for iVitri Straw is MQK.

Other Devices by Reprobitech Corp.

K162640iVitri EZ

Related Devices (Code: MQK)

K162051CryotecReprolife, Inc. K153027Cryotop USKitazato Biopharma Co., Ltd. K162640iVitri EZReprobitech Corp. K162833VitriGuardOrigio A/S K181469Cryotop®US-flash and Cryotop®US-scoopKitazato Corporation K180740VitriGuardOrigio A/S

Official Source

View on FDA Database →

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

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