Salix Central
K-Number: K243038 · 2025-03-27
Device Summary
Frequently Asked Questions
What is the Salix Central?
Salix Central is a medical device that received FDA 510(k) clearance on 2025-03-27. The listed applicant is Artrya Limited. The 510(k) number is K243038.
When did Salix Central receive FDA 510(k) clearance?
Salix Central received FDA 510(k) clearance on 2025-03-27, under 510(k) number K243038.
Who is the listed applicant for Salix Central?
The FDA 510(k) record lists Artrya Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Salix Central?
The FDA product code for Salix Central is QIH.
Other records listing Artrya Limited as applicant
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.
Related Devices (Code: QIH)
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.