Technicon DPA-1 Immunoglobulin a

FDA 510(k) K883492 · Technicon Instruments Corp.

Substantially Equivalent

510(k) numberK883492

Submission

Device name
Technicon DPA-1 Immunoglobulin a
Applicant
Technicon Instruments Corp.
Tarrytown, NY, US
Received
August 16, 1988
Decision date
September 22, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CZP – Iga, Antigen, Antiserum, Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5510
Specialty
Immunology

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K040435Roche Diagnostics Tina-Quant Iga GEN.2CZP · Special Roche Diagnostics Corp.03/10/2004SE
K024038N Latex IgaCZP · Traditional Dade Behring, Inc.02/13/2003SE
K993927Wako Iga Ii-Ha, Immunoglobulin Calibrator Set, Immunoglobulin StandradCZP · Traditional Wako Chemicals USA, Inc.01/14/2000SE
K983359IgaCZP · Traditional Abbott Laboratories11/04/1998SE
K962200Quantex IgaCZP · Traditional Instrumentation Laboratory CO09/25/1996SE
K955794Iga Immunoturbidimetric & CalibratorCZP · Traditional Randox Laboratories, Ltd.04/05/1996SE
K955907Boehringer Mannheim Iga AssayCZP · Traditional Boehringer Mannheim Corp.02/09/1996SE
K952309N Latex IgaCZP · Traditional Behring Diagnostics, Inc.06/20/1995SE

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Questions and answers

When was Technicon DPA-1 Immunoglobulin a cleared by the FDA?

Technicon DPA-1 Immunoglobulin a (K883492) received a 510(k) decision of Substantially Equivalent on September 22, 1988, 37 days after the submission was received.

What is the product code of K883492?

The FDA product code is CZP – Iga, Antigen, Antiserum, Control, a Class II (moderate risk) device regulated under 21 CFR 866.5510.