Salicylate Test

FDA 510(k) K843180 · Sclavo, Inc.

Substantially Equivalent

510(k) numberK843180

Submission

Device name
Salicylate Test
Applicant
Sclavo, Inc.
Mchenry, IL, US
Received
August 13, 1984
Decision date
September 7, 1984
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

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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 Test cleared by the FDA?

Salicylate Test (K843180) received a 510(k) decision of Substantially Equivalent on September 7, 1984, 25 days after the submission was received.

What is the product code of K843180?

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