Technicon DPA-1(TM) System

FDA 510(k) K882153 · Technicon Instruments Corp.

Substantially Equivalent

510(k) numberK882153

Submission

Device name
Technicon DPA-1(TM) System
Applicant
Technicon Instruments Corp.
Tarrytown, NY, US
Received
May 23, 1988
Decision date
August 4, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DCF – Albumin, Antigen, Antiserum, Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5040
Specialty
Immunology

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Questions and answers

When was Technicon DPA-1(TM) System cleared by the FDA?

Technicon DPA-1(TM) System (K882153) received a 510(k) decision of Substantially Equivalent on August 4, 1988, 73 days after the submission was received.

What is the product code of K882153?

The FDA product code is DCF – Albumin, Antigen, Antiserum, Control, a Class II (moderate risk) device regulated under 21 CFR 866.5040.