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

Antiserum, Fluorescent, Epstein-Barr Virus (JRY): 3 FDA-registered makers in 1 country

3 establishments in 1 country are registered with the FDA to make Antiserum, Fluorescent, Epstein-Barr Virus (product code JRY, Class 1, 21 CFR 866.3235). 3 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 9 510(k) clearances under this code, the latest on April 29, 2005, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
JRY
Device class
1
Regulation
866.3235
Medical specialty
Microbiology

Makers by country

CountryMakers
United States3

Makers of Antiserum, Fluorescent, 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
Zeus Scientific LLCBranchburg, NJ, United StatesManufacturer, Repackager or relabeler3April 29, 2005000api.fda.gov
Bion Enterprises, Ltd.Des Plaines, IL, United StatesContract manufacturer, Manufacturer1August 31, 1989000api.fda.gov
Diagnostic Automation/ Cortez Diagnostics Inc,.Woodland Hills, CA, United StatesManufacturer1May 27, 1981000api.fda.gov

Updated April 29, 2005. 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.