Documento fuente o registro público
FDA 510(k) K202641 — DNA/RNA Shield Collection Tube
FDA 510(k) index record K202641. Device: DNA/RNA Shield Collection Tube. Applicant as listed: Zymo Research. Decision date: 2020-12-14.
Fuente
"device_name": "DNA/RNA Shield Collection Tube"
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Review and references
Automated FDA record verification
2026-10-20
2026-10-20
professional use
FDA 510(k) public index record K202641.
Device name: DNA/RNA Shield Collection Tube. Applicant as listed: Zymo Research.
Decision date: 2020-12-14. Decision wording: Substantially Equivalent.
Product code: QBD. Regulation: 21 CFR 866.2950. 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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