Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

SCA · Predicate Candidate Screening

12 FDA 510(k) clearances under this product code; the 50 most recent screened below.

122 daysmedian FDA review time
246 days90th percentile
12clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K261212Flowflex Plus RSV + Flu A/B + COVID Rapid TestACON Laboratories, Inc.2026-07-10870
K251085iHealth Flu A&B/COVID-19/RSV Rapid Test; iHealth Flu A&B/COVIhealth Labs, Inc.2025-12-122470
K251092iHealth Flu A&B/COVID-19 Rapid Test; iHealth Flu A&B/COVID-1Ihealth Labs, Inc.2025-12-122460
K251538Status™ COVID-19/Flu A&BPrinceton BioMeditech Corp.2025-11-141790
K251749Flowflex Plus RSV + Flu A/B + COVID Home TestACON Laboratories, Inc.2025-10-221380
K251604CareSuperb COVID-19/Flu A&B Antigen Combo Home TestAccess Bio, Inc.2025-08-22870
K251563WELLlife Flu A&B Home Test; WELLlife Influenza A&B TestWondfo USA Co, Ltd.2025-08-20900
K243561Nano-Check Influenza+COVID-19 Dual TestNano-Ditech Corporation2025-06-172110
K250377Flowflex Plus COVID-19 + Flu A/B Home TestACON Laboratories, Inc.2025-05-10890
K243256WELLlife™ COVID-19 / Influenza A&B Home Test; WELLlife™ COVIWondfo USA Co, Ltd.2025-01-16930
K243262QuickFinder COVID-19/Flu Antigen Self Test / QuickFinder COVOsang, LLC2025-01-13900
DEN240029Healgen Rapid Check COVID-19/Flu A&B Antigen TestHealgen2024-10-071220

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda