Emit Cad Procainamide Assay

FDA 510(k) K832718 · Syva Co.

Substantially Equivalent

510(k) numberK832718

Submission

Device name
Emit Cad Procainamide Assay
Applicant
Syva Co.
Mchenry, IL, US
Received
August 12, 1983
Decision date
September 12, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LAR – Enzyme Immunoassay, Procainamide
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3320
Specialty
Clinical Toxicology

Other 510(k)s with product code LAR

510(k)DeviceApplicantDecision
K060773Online TDM ProcainamideLAR · Traditional Roche Diagnostics Corp.08/23/2006SE
K032573Dimension Procainamide (Proc) Flex Reagent Cartridge Method, Model DF110LAR · Traditional Dade Behring, Inc.10/31/2003SE
K010812Emit 2000 Procainamide Assay, Model OSR4K229LAR · Special Syva Co., Dade Behring, Inc.04/13/2001SE
K971716Procainamide Assay for the Bayer Immuno 1 SystemLAR · Traditional Bayer Corp.06/27/1997SE
K963306Cedia N-Acetylprocainamide AssayLAR · Traditional Boehringer Mannheim Corp.10/29/1996SE
K962099Cedia Procainamide AssayLAR · Traditional Boehringer Mannheim Corp.08/27/1996SE
K962463Procainamide Enzyme ImmunoassayLAR · Traditional Diagnostic Reagents, Inc.08/14/1996SE
K955444Abbott Axsm Procainamide AssayLAR · Traditional Abbott Laboratories04/02/1996SE
K951434Opus ProcainamideLAR · Traditional Behring Diagnostics, Inc.07/03/1995SE
K942847Cobas(R)-Fp Reagent for Procainamide/CalibratorLAR · Traditional Roche Diagnostic Systems, Inc.12/02/1994SE

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Questions and answers

When was Emit Cad Procainamide Assay cleared by the FDA?

Emit Cad Procainamide Assay (K832718) received a 510(k) decision of Substantially Equivalent on September 12, 1983, 31 days after the submission was received.

What is the product code of K832718?

The FDA product code is LAR – Enzyme Immunoassay, Procainamide, a Class II (moderate risk) device regulated under 21 CFR 862.3320.