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LIAISON® XL MUREX Anti-HDV - LIAISON® XL MUREX Anti-HDV (318260)
FDA 510(k)Class II (US FDA 510(k))
510(k) DEN250032
Identifiers
- 510(k) Number
- DEN250032 FDA 510(k)
- FDA Product Code
- SGW FDA 510(k)
- Models / Variants
- LIAISON® XL MUREX Anti-HDV (318260) FDA 510(k)LIAISON® XL MUREX Control Anti-HDV (318261) FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 866.3176 FDA 510(k)
- Regulation Number
- 866.3176 FDA 510(k)
- Advisory Committee
- Immunology FDA 510(k)
- FDA Decision
- DENG FDA 510(k)
LIAISON® XL MUREX Anti-HDV - LIAISON® XL MUREX Anti-HDV (318260) by Diasorin Inc. — Class II — FDA_510K — listed in FDA 510(k) — 2 models
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | DEN250032 | Class II | Active |
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Manufacturer
- Manufacturer
- Diasorin Inc.
- FDA Applicant
- DiaSorin, Inc.
Sources (1)
- FDA 510(k) DEN250032 24 fields · synced Jun 18, 2026