TECHNICON CHEM 1 CLINICAL ANALYZER FOR URINE URIC— 510(k) K901693

Name: FDA 510(k) clearance K901693
Creator: U.S. Food and Drug Administration
Published: 1990-04-25

Substantially Equivalent

Technicon Instruments Corp.

FDA 510(k) clearance K901693 for TECHNICON CHEM 1 CLINICAL ANALYZER FOR URINE URIC, Substantially Equivalent on 1990-04-25. Applicant: Technicon Instruments Corp.. Device class: 1.

Clearance details

Applicant: Technicon Instruments Corp.
Product code: Code KNK
Device class: Class 1
Regulation: 21 CFR 862.1775
Advisory panel: Clinical Chemistry
Date received: 1990-04-11
Decision date: 1990-04-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tarrytown, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KNK

view all

K102568 — URIC ACID MODEL 3P392011-05-06
K062862 — OLYMPUS URIC ACID REAGENT, MODEL OSR6X982007-04-06
K040467 — VITALAB URIC ACID REAGENT2004-03-08
K031044 — ATAC PAK URIC ACID REAGENT AND ATAC CALIBRATOR2003-07-15
K022096 — URIC ACID ASSAY FOR THE ADVIA INTEGRATED MODULAR SYSTEM2003-03-18

More clearances from Technicon Instruments Corp.

view all

K914511 — TECHNICON AXON(TM) SYSTEM METHODS ANYALYE HDL CHOL1991-11-27
K914888 — TECHNICON CHEM 1(TM) SYST (GEN2 SYST)1991-11-27
K914025 — TECHNICON AXON(TM) SYSTEMS, ALT(P 5-P)/AST(P 5-P)1991-11-22
K912616 — TECHNICON IMMUNO 1 TM SYSTEM ADDITIONAL ANALYTES1991-09-25
K912413 — CHEM-LINK DATA BASE MANAGER1991-07-01

Data sourced from openFDA. This site is unofficial and independent of the FDA.