Accusign DOA2, Doa, Bar/Bzo, Biosign DOA2, Bar/Bzo, Status DS Bar/Bzo, Syva Rapidtest D.A.U. 2 Bar/Bzo

FDA 510(k) K991082 · Princeton BioMeditech Corp.

Substantially Equivalent

510(k) numberK991082

Submission

Device name
Accusign DOA2, Doa, Bar/Bzo, Biosign DOA2, Bar/Bzo, Status DS Bar/Bzo, Syva Rapidtest D.A.U. 2 Bar/Bzo
Applicant
Princeton BioMeditech Corp.
Monmouth Junction, NJ, US
Received
March 26, 1999
Decision date
April 15, 1999
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
DIS – Enzyme Immunoassay, Barbiturate
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3150
Specialty
Clinical Toxicology

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Questions and answers

When was Accusign DOA2, Doa, Bar/Bzo, Biosign DOA2, Bar/Bzo, Status DS Bar/Bzo, Syva Rapidtest D.A.U. 2 Bar/Bzo cleared by the FDA?

Accusign DOA2, Doa, Bar/Bzo, Biosign DOA2, Bar/Bzo, Status DS Bar/Bzo, Syva Rapidtest D.A.U. 2 Bar/Bzo (K991082) received a 510(k) decision of Substantially Equivalent on April 15, 1999, 20 days after the submission was received.

What is the product code of K991082?

The FDA product code is DIS – Enzyme Immunoassay, Barbiturate, a Class II (moderate risk) device regulated under 21 CFR 862.3150.