TECHNICON DPA-1 (TM) CRP METHOD— 510(k) K892198

Name: FDA 510(k) clearance K892198
Creator: U.S. Food and Drug Administration
Published: 1989-05-09

Substantially Equivalent

Technicon Instruments Corp.

FDA 510(k) clearance K892198 for TECHNICON DPA-1 (TM) CRP METHOD, Substantially Equivalent on 1989-05-09. Applicant: Technicon Instruments Corp.. Device class: 2.

Clearance details

Applicant: Technicon Instruments Corp.
Product code: Code DCK
Device class: Class 2
Regulation: 21 CFR 866.5270
Advisory panel: Immunology
Date received: 1989-04-03
Decision date: 1989-05-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tarrytown, NY, US

Download summary PDF View on FDA.gov ↗

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