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Data / Medical devices / Cardiovascular Machine Learning-Based Notification Software

Cardiovascular Machine Learning-Based Notification Software (QXO): 3 FDA-registered makers in 2 countries

3 establishments in 2 countries are registered with the FDA to make Cardiovascular Machine Learning-Based Notification Software (product code QXO, Class 2, 21 CFR 870.2380). 3 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 2 510(k) clearances under this code, the latest on June 8, 2026, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
QXO
Device class
2
Regulation
870.2380
Medical specialty
Cardiovascular

Makers by country

CountryMakers
United States2
Israel1

Makers of Cardiovascular Machine Learning-Based Notification Software

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Pathwai, IncNew York, NY, United StatesManufacturer1June 8, 2026000api.fda.gov
Viz.ai, Inc.Cary, NC, United StatesComplaint file establishment, Specification developer1August 3, 2023000api.fda.gov
Viz.ai Israel LtdTel Aviv, IsraelManufacturer1August 3, 2023000api.fda.gov

Updated June 8, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.