Theophylline Fpia Reagent Set and Calibrators

FDA 510(k) K942192 · Sigma Diagnostics, Inc.

Substantially Equivalent

510(k) numberK942192

Submission

Device name
Theophylline Fpia Reagent Set and Calibrators
Applicant
Sigma Diagnostics, Inc.
St. Louis, MO, US
Received
May 4, 1994
Decision date
July 13, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
LER – Fluorescent Immunoassay, Theophylline
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3880
Specialty
Clinical Toxicology

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K863475Theofast(Tm) Test PackageLER · Traditional 3M Company11/05/1986SE
K842585Theophylline Kit Fluorescence Polariza-LER · Traditional Windsor Laboratories, Inc.09/26/1984SE
K840758Immpulse Theophylline Assay ReagentsLER · Traditional Paragon Diagnostics, Inc.04/04/1984SE
K833070TDX TheophyllineLER · Traditional Abbott Laboratories11/14/1983SE
K831514Amwa Tda Theophylline TestLER · Traditional Miles Laboratories, Inc.06/30/1983SE
K823576Cobas Standard for Total ProteinLER · Traditional Hoffmann-La Roche, Inc.01/07/1983SE
K820397Amerifluor Theophylline Fluorescent ImmLER · Traditional American Diagnostic Corp.03/02/1982SE

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Questions and answers

When was Theophylline Fpia Reagent Set and Calibrators cleared by the FDA?

Theophylline Fpia Reagent Set and Calibrators (K942192) received a 510(k) decision of Substantially Equivalent on July 13, 1994, 70 days after the submission was received.

What is the product code of K942192?

The FDA product code is LER – Fluorescent Immunoassay, Theophylline, a Class II (moderate risk) device regulated under 21 CFR 862.3880.