SchurSign Tissue Marker
K-Number: K230836 · 2024-01-23
Device Summary
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. The listed applicant is Surgmark GmbH. The 510(k) number is K230836.
When did SchurSign Tissue Marker receive FDA 510(k) clearance?
SchurSign Tissue Marker received FDA 510(k) clearance on 2024-01-23, under 510(k) number K230836.
Who is the listed applicant for SchurSign Tissue Marker?
The FDA 510(k) record lists Surgmark GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SchurSign Tissue Marker?
The FDA product code for SchurSign Tissue Marker is NEU.
Related Devices (Code: NEU)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.