Ames Tda Valproic Acid Test

FDA 510(k) K830789 · Miles Laboratories, Inc.

Substantially Equivalent

510(k) numberK830789

Submission

Device name
Ames Tda Valproic Acid Test
Applicant
Miles Laboratories, Inc.
Walker, MI, US
Received
March 14, 1983
Decision date
April 12, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LEG – Enzyme Immunoassay, Valproic Acid
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3645
Specialty
Clinical Toxicology

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K042807Advia Ims Valproic Acid MethodLEG · Traditional Bayer Healthcare, LLC02/08/2005SE
K042476Vitros Chemistry Products Valp Reagent; Vitro Chemistry Products Calibrator Kit 12…LEG · Traditional Ortho-Clinical Diagnostics, Inc.12/01/2004SE
K032049Roche Online TDM Valproic AcidLEG · Traditional Roche Diagnostics Corp.08/22/2003SE
K031870Synchron Systems Valproic Acid (V-Pa) ReagentLEG · Special Beckman Coulter, Inc.07/15/2003SE
K030405QMS / Multigent Valproic Acid Reagent, Part #396075LEG · Traditional Seradyn04/28/2003SE
K011649Randox Valproic AcidLEG · Traditional Randox Laboratories, Ltd.01/15/2002SE
K011947Emit 2000 Valproic Acid Assay, Model OSR4G229ULLEG · Special Syva Co.07/02/2001SE
K002551Emit 2000 Valproic Acid Assay, Emit 2000 Valproic Acid Calibrators, Model 4G019UL, 4G109ULLEG · Traditional Dade Behring, Inc.10/11/2000SE

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Questions and answers

When was Ames Tda Valproic Acid Test cleared by the FDA?

Ames Tda Valproic Acid Test (K830789) received a 510(k) decision of Substantially Equivalent on April 12, 1983, 29 days after the submission was received.

What is the product code of K830789?

The FDA product code is LEG – Enzyme Immunoassay, Valproic Acid, a Class II (moderate risk) device regulated under 21 CFR 862.3645.