LIAISON Anti-HAV; LIAISON XS
K-Number: K223403 · 2022-12-09
Device Summary
Frequently Asked Questions
What is the LIAISON Anti-HAV; LIAISON XS?
LIAISON Anti-HAV; LIAISON XS is a medical device that received FDA 510(k) clearance on 2022-12-09. The listed applicant is DiaSorin, Inc.. The 510(k) number is K223403.
When did LIAISON Anti-HAV; LIAISON XS receive FDA 510(k) clearance?
LIAISON Anti-HAV; LIAISON XS received FDA 510(k) clearance on 2022-12-09, under 510(k) number K223403.
Who is the listed applicant for LIAISON Anti-HAV; LIAISON XS?
The FDA 510(k) record lists DiaSorin, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIAISON Anti-HAV; LIAISON XS?
The FDA product code for LIAISON Anti-HAV; LIAISON XS is LOL.
Other records listing DiaSorin, Inc. 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: LOL)
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.