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FDA 510(k)

FlowArt Valve for Vial Access

K-Number: K232987 · 2024-06-26

ApplicantAsset Medikal Tasarim Sanayi VE Ticaret A.S.
Decision Date2024-06-26
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FlowArt Valve for Vial Access is a medical device manufactured by Asset Medikal Tasarim Sanayi VE Ticaret A.S.. It received FDA 510(k) clearance on 2024-06-26 under approval number K232987. The device is classified under product code LHI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FlowArt Valve for Vial Access?

FlowArt Valve for Vial Access is a medical device that received FDA 510(k) clearance on 2024-06-26. It is manufactured by Asset Medikal Tasarim Sanayi VE Ticaret A.S.. The 510(k) number is K232987.

When was FlowArt Valve for Vial Access approved by the FDA?

FlowArt Valve for Vial Access received FDA 510(k) clearance on 2024-06-26, under approval number K232987.

What company makes FlowArt Valve for Vial Access?

FlowArt Valve for Vial Access is manufactured by Asset Medikal Tasarim Sanayi VE Ticaret A.S..

What is the FDA product code for FlowArt Valve for Vial Access?

The FDA product code for FlowArt Valve for Vial Access is LHI.

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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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