Salicylate Assay Kit

FDA 510(k) K831336 · Quantimetrix Corp.

Substantially Equivalent

510(k) numberK831336

Submission

Device name
Salicylate Assay Kit
Applicant
Quantimetrix Corp.
Mchenry, IL, US
Received
April 25, 1983
Decision date
July 7, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DKJ – Colorimetry, Salicylate
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3830
Specialty
Clinical Toxicology

Other 510(k)s with product code DKJ

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K093939Advia Chemistry Salicylate ReagentDKJ · Traditional Siemens Healthcare Diagnostics05/19/2010SE
K042329Salicylate-Sl AssayDKJ · Traditional Diagnostic Chemicals , Ltd.12/27/2004SE
K020794Salicylate Assay for the Advia Integrated Modular SystemDKJ · Traditional Bayer Diagnostics Corp.07/11/2002SE
K014173Synchron Systems Salicylate Reagent and CalibratorDKJ · Traditional Beckman Coulter, Inc.02/15/2002SE
K011878Emit (R) Tox Salicylic Assay, Model 7SO19UL, Emit (R) Tox Salicylic Acid Calibrators…DKJ · Traditional Syva Co.08/13/2001SE
K981872Salicylate-Sl Assay Catalogue Number 511-20,511-40DKJ · Traditional Diagnostic Chemicals , Ltd.06/29/1998SE
K980032Salicylate Assay (Ace), Catalogue Number 501-71DKJ · Traditional Diagnostic Chemicals , Ltd.03/02/1998SE
K964715Paramax Salicylate ReagentDKJ · Traditional Dade Intl., Inc.04/25/1997SE
K961131Salicylate AssayDKJ · Traditional Diagnostic Reagents, Inc.04/29/1996SE
K951290Axsym SalicylateDKJ · Traditional Abbott Laboratories08/08/1995SE

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Questions and answers

When was Salicylate Assay Kit cleared by the FDA?

Salicylate Assay Kit (K831336) received a 510(k) decision of Substantially Equivalent on July 7, 1983, 73 days after the submission was received.

What is the product code of K831336?

The FDA product code is DKJ – Colorimetry, Salicylate, a Class II (moderate risk) device regulated under 21 CFR 862.3830.