Source document or public record
FDA 510(k) K221664 — CLEARinse CTS Specimen Collection and Transport System
FDA 510(k) index record K221664. Device: CLEARinse CTS Specimen Collection and Transport System. Applicant as listed: Aardvark Medical, Inc.. Decision date: 2023-07-03.
Source
"device_name": "CLEARinse CTS Specimen Collection and Transport System"
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 K221664.
Device name: CLEARinse CTS Specimen Collection and Transport System. Applicant as listed: Aardvark Medical, Inc..
Decision date: 2023-07-03. 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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