FDA 510(k)

SchurSign Tissue Marker

K-Number: K230836 · 2024-01-23

Decision Date2024-01-23

Product CodeNEU

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

SchurSign Tissue Marker is a medical device manufactured by Surgmark GmbH. It received FDA 510(k) clearance on 2024-01-23 under approval number K230836. The device is classified under product code NEU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SchurSign Tissue Marker?

SchurSign Tissue Marker is a medical device that received FDA 510(k) clearance on 2024-01-23. It is manufactured by Surgmark GmbH. The 510(k) number is K230836.

When was SchurSign Tissue Marker approved by the FDA?

SchurSign Tissue Marker received FDA 510(k) clearance on 2024-01-23, under approval number K230836.

What company makes SchurSign Tissue Marker?

SchurSign Tissue Marker is manufactured by Surgmark GmbH.

What is the FDA product code for SchurSign Tissue Marker?

The FDA product code for SchurSign Tissue Marker is NEU.

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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.