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Data / Medical devices / Radioimmunoassay, Barbiturate

Radioimmunoassay, Barbiturate (DKN): 4 FDA-registered makers in 1 country

4 establishments in 1 country are registered with the FDA to make Radioimmunoassay, Barbiturate (product code DKN, Class 2, 21 CFR 862.3150). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 4 510(k) clearances under this code, the latest on October 30, 1991, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
DKN
Device class
2
Regulation
862.3150
Medical specialty
Clinical Toxicology

Makers by country

CountryMakers
United States4

Makers of Radioimmunoassay, Barbiturate

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
Princeton Biomeditech Corp.Monmouth Jct, NJ, United StatesManufacturer0000api.fda.gov
Princeton BioMeditech Corp.Plainsboro, NJ, United StatesManufacturer0000api.fda.gov
Princeton BioMeditech Corp.Skillman, NJ, United StatesManufacturer0000api.fda.gov
Siemens Healthcare Diagnostics Inc.Newark, DE, United StatesManufacturer0000api.fda.gov

Updated October 30, 1991. 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.