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Data / Medical devices / Filter, Blood, Cardiotomy Suction Line, Cardiopulmonary Bypass

Filter, Blood, Cardiotomy Suction Line, Cardiopulmonary Bypass (JOD): 3 FDA-registered makers in 2 countries

3 establishments in 2 countries are registered with the FDA to make Filter, Blood, Cardiotomy Suction Line, Cardiopulmonary Bypass (product code JOD, Class 2, 21 CFR 870.4270). 1 of them has a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 12 510(k) clearances under this code, the latest on March 28, 2000, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
JOD
Device class
2
Regulation
870.4270
Medical specialty
Cardiovascular

Makers by country

CountryMakers
United States2
Mexico1

Makers of Filter, Blood, Cardiotomy Suction Line, Cardiopulmonary Bypass

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
GVS TM, Inc.Covina, CA, United StatesManufacturer1February 29, 1988000api.fda.gov
Medtronic Perfusion SystemsMinneapolis, MN, United StatesManufacturer0000api.fda.gov
Medtronic Mexico S. de R.L. de CVTijuana Baja California, MexicoManufacturer0000api.fda.gov

Updated March 28, 2000. 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.