Source document or public record
FDA 510(k) K202755 — Simplexa Congenital CMV Direct and Simplexa Congenital CMV Positive Control Pack
FDA 510(k) index record K202755. Device: Simplexa Congenital CMV Direct and Simplexa Congenital CMV Positive Control Pack. Applicant as listed: Diasorin Molecular, LLC. Decision date: 2022-11-05.
Source
"device_name": "Simplexa Congenital CMV Direct and Simplexa Congenital CMV Positive Control Pack"
This entry describes what the document covers; the document itself is the authority. Listing it is not agreement with its conclusions.
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2026-10-20
2026-10-20
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FDA 510(k) public index record K202755.
Device name: Simplexa Congenital CMV Direct and Simplexa Congenital CMV Positive Control Pack. Applicant as listed: Diasorin Molecular, LLC.
Decision date: 2022-11-05. Decision wording: Substantially Equivalent.
Product code: QDZ. Regulation: 21 CFR 866.3181. Medical specialty: Microbiology.
This page reproduces regulator index metadata. The applicant field identifies the submitter and is not a manufacturer identity check. Consult the original FDA record for the decision and associated documents; this index does not verify current commercial availability or clinical performance.
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