Theophylline Fpia Reagent Set

FDA 510(k) K870952 · Sigma Diagnostics, Inc.

Substantially Equivalent

510(k) numberK870952

Submission

Device name
Theophylline Fpia Reagent Set
Applicant
Sigma Diagnostics, Inc.
St. Louis, MO, US
Received
March 10, 1987
Decision date
March 31, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

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

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K020740Roche Online TheophyllineKLS · Traditional Roche Diagnostics Corp.04/16/2002SE
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K013272Acs: 180 and Advia Centaur Theophylline 2 AssayKLS · Special Bayer Corp.10/25/2001SE
K011166Modification to Emit 2000 Theophylline Assay, Model Osr 4P229KLS · Special Syva Co., Dade Behring, Inc.05/10/2001SE
K993029Abbott Aeroset Theophylline Assay and Calibrators; Models 1E09 and 6E89KLS · Traditional Syva Co.01/27/2000SE
K973583Ace Theophylline Reagent, Theo CalibratorsKLS · Traditional Schiapparelli Biosystems, Inc.11/12/1997SE
K972495Accumeter Theophylline TestKLS · Traditional Chemtrak, Inc.10/10/1997SE
K961462Cedia Theophylline AssayKLS · Traditional Boehringer Mannheim Corp.06/27/1996SE

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Questions and answers

When was Theophylline Fpia Reagent Set cleared by the FDA?

Theophylline Fpia Reagent Set (K870952) received a 510(k) decision of Substantially Equivalent on March 31, 1987, 21 days after the submission was received.

What is the product code of K870952?

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