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Data / Medical devices / Medium-Term Adjunctive Predictive Cardiovascular Indicator / United States

FDA-registered makers of Medium-Term Adjunctive Predictive Cardiovascular Indicator in the United States: 5 establishments

5 establishments in the United States are registered with the FDA to make Medium-Term Adjunctive Predictive Cardiovascular Indicator (product code QNL). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Medium-Term Adjunctive Predictive Cardiovascular Indicator
Product code
QNL
Country
United States

Makers of Medium-Term Adjunctive Predictive Cardiovascular Indicator in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
AgilemdCupertino, CA, United StatesComplaint file establishment, Manufacturer1June 21, 2024000api.fda.gov
Epic Systems CorporationVerona, WI, United StatesManufacturer1September 18, 2026000api.fda.gov
AirStrip Technologies, Inc.San Antonio, TX, United StatesManufacturer0000api.fda.gov
Becton, Dickinson And CompanyIrvine, CA, United StatesSpecification developer0000api.fda.gov
Benchmark Electronics, Inc.Winona, MN, United StatesContract manufacturer0000api.fda.gov

Updated November 2, 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.