Source document or public record
FDA 510(k) K220801 — ID Now Instrument, ID Now Influenza A & B 2, ID NOW Strep A 2
FDA 510(k) index record K220801. Device: ID Now Instrument, ID Now Influenza A & B 2, ID NOW Strep A 2. Applicant as listed: Abbott Diagnostics Scarborough, Inc.. Decision date: 2022-06-24.
Source
"device_name": "ID Now Instrument, ID Now Influenza A & B 2, ID NOW Strep A 2"
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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Automated FDA record verification
2026-10-20
2026-10-20
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FDA 510(k) public index record K220801.
Device name: ID Now Instrument, ID Now Influenza A & B 2, ID NOW Strep A 2. Applicant as listed: Abbott Diagnostics Scarborough, Inc..
Decision date: 2022-06-24. Decision wording: Substantially Equivalent.
Product code: OZE. Regulation: 21 CFR 866.3980. 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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