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Data / Medical devices / Antiserum, Cf, Epstein-Barr Virus

Antiserum, Cf, Epstein-Barr Virus (GNP): 4 FDA-registered makers in 1 country

4 establishments in 1 country are registered with the FDA to make Antiserum, Cf, Epstein-Barr Virus (product code GNP, Class 1, 21 CFR 866.3235). 4 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 20 510(k) clearances under this code, the latest on June 13, 2002, and lists 2 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
GNP
Device class
1
Regulation
866.3235
Medical specialty
Microbiology

Makers by country

CountryMakers
United States4

Makers of Antiserum, Cf, Epstein-Barr Virus

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
Gold Standard Diagnostics, LLCDavis, CA, United StatesRepackager or relabeler, Specification developer2February 16, 1999000api.fda.gov
IMMUNO CONCEPTS, NA, Ltd.Sacramento, CA, United StatesManufacturer2August 30, 1988000api.fda.gov
Hemagen Diagnostics, Inc.Baltimore, MD, United StatesManufacturer1May 5, 1981000api.fda.gov
Trinity Biotech USAJamestown, NY, United StatesManufacturer1April 28, 1989000api.fda.gov

Updated June 13, 2002. 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.