FDA 510(k)

ARTSMedia Semen Wash Medium

K-Number: K241095 · 2024-12-18

Decision Date2024-12-18

Product CodeMQL

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

ARTSMedia Semen Wash Medium is a medical device manufactured by Artsmedia Denmark Aps. It received FDA 510(k) clearance on 2024-12-18 under approval number K241095. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTSMedia Semen Wash Medium?

ARTSMedia Semen Wash Medium is a medical device that received FDA 510(k) clearance on 2024-12-18. It is manufactured by Artsmedia Denmark Aps. The 510(k) number is K241095.

When was ARTSMedia Semen Wash Medium approved by the FDA?

ARTSMedia Semen Wash Medium received FDA 510(k) clearance on 2024-12-18, under approval number K241095.

What company makes ARTSMedia Semen Wash Medium?

ARTSMedia Semen Wash Medium is manufactured by Artsmedia Denmark Aps.

What is the FDA product code for ARTSMedia Semen Wash Medium?

The FDA product code for ARTSMedia Semen Wash Medium is MQL.

Other Devices by Artsmedia Denmark Aps

K220715ARTSMedia In Vitro Culture Medium (AM-IVC Medium) K241132ARTSMedia Oocyte Aspiration Medium (502020, 502050, 502100)

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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.