Oti Benzodiazepines Intercept Micro-Plate Eia Model #1110I

FDA 510(k) K013882 · OraSure Technologies, Inc.

Substantially Equivalent

510(k) numberK013882

Submission

Device name
Oti Benzodiazepines Intercept Micro-Plate Eia Model #1110I
Applicant
OraSure Technologies, Inc.
Bethlehem, PA, US
Received
November 23, 2001
Decision date
April 17, 2002
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JXM – Enzyme Immunoassay, Benzodiazepine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3170
Specialty
Clinical Toxicology

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Questions and answers

When was Oti Benzodiazepines Intercept Micro-Plate Eia Model #1110I cleared by the FDA?

Oti Benzodiazepines Intercept Micro-Plate Eia Model #1110I (K013882) received a 510(k) decision of Substantially Equivalent on April 17, 2002, 145 days after the submission was received.

What is the product code of K013882?

The FDA product code is JXM – Enzyme Immunoassay, Benzodiazepine, a Class II (moderate risk) device regulated under 21 CFR 862.3170.