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FDA 510(k)

Follicle Aspiration Set, Reduced Single Lumen

K-Number: K172050 · 2017-11-21

ApplicantVitrolife Sweden AB
Decision Date2017-11-21
Product CodeMQE
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Follicle Aspiration Set, Reduced Single Lumen is a medical device manufactured by Vitrolife Sweden AB. It received FDA 510(k) clearance on 2017-11-21 under approval number K172050. The device is classified under product code MQE. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Follicle Aspiration Set, Reduced Single Lumen?

Follicle Aspiration Set, Reduced Single Lumen is a medical device that received FDA 510(k) clearance on 2017-11-21. It is manufactured by Vitrolife Sweden AB. The 510(k) number is K172050.

When was Follicle Aspiration Set, Reduced Single Lumen approved by the FDA?

Follicle Aspiration Set, Reduced Single Lumen received FDA 510(k) clearance on 2017-11-21, under approval number K172050.

What company makes Follicle Aspiration Set, Reduced Single Lumen?

Follicle Aspiration Set, Reduced Single Lumen is manufactured by Vitrolife Sweden AB.

What is the FDA product code for Follicle Aspiration Set, Reduced Single Lumen?

The FDA product code for Follicle Aspiration Set, Reduced Single Lumen is MQE.

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Other Devices by Vitrolife Sweden AB

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Related Devices (Code: MQE)

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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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