Data / Medical devices / Angiography/Angioplasty Kit

Angiography/Angioplasty Kit (OEQ): 24 FDA-registered makers in 8 countries

24 establishments in 8 countries are registered with the FDA to make Angiography/Angioplasty Kit (product code OEQ, Class 2, 21 CFR 870.1650). 0 of them have a 510(k) clearance or PMA approval on file and 2 have a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 46 recall events (4 Class I). FDA data exported November 2, 2026.

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Product code

OEQ

Device class

2

Regulation

870.1650

Medical specialty

Cardiovascular

Makers by country

Makers of Angiography/Angioplasty Kit

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.

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.