LIAISON® XL MUREX Anti-HDV (318260); LIAISON® XL MUREX Control Anti-HDV (318261)— 510(k) DEN250032

Name: FDA 510(k) clearance DEN250032
Creator: U.S. Food and Drug Administration
Published: 2025-12-23

Unknown

DiaSorin, Inc.

FDA 510(k) clearance DEN250032 for LIAISON® XL MUREX Anti-HDV (318260); LIAISON® XL MUREX Control Anti-HDV (318261), Unknown on 2025-12-23. Applicant: DiaSorin, Inc.. Device class: 2.

Clearance details

Applicant: DiaSorin, Inc.
Product code: Code SGW
Device class: Class 2
Regulation: 21 CFR 866.3176
Advisory panel: Immunology
Date received: 2025-07-30
Decision date: 2025-12-23
Decision: Unknown
Clearance type: Direct
Location: Stillwater, MN, US

View on FDA.gov ↗

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