RDW PARAMETER FOR THE TECHNICON H6000— 510(k) K834026

Name: FDA 510(k) clearance K834026
Creator: U.S. Food and Drug Administration
Published: 1984-01-30

Substantially Equivalent

Technicon Instruments Corp.

FDA 510(k) clearance K834026 for RDW PARAMETER FOR THE TECHNICON H6000, Substantially Equivalent on 1984-01-30. Applicant: Technicon Instruments Corp.. Device class: 2.

Clearance details

Applicant: Technicon Instruments Corp.
Product code: Code GKL
Device class: Class 2
Regulation: 21 CFR 864.5200
Advisory panel: Hematology
Date received: 1983-11-22
Decision date: 1984-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GKL

view all

K152776 — Glocyte Automated Cell Counter System2016-05-27
K091539 — IQ 200 URINE ANALIZER BODY FLUIDS MODULE2010-08-31
K071652 — HEMOCUE WBC SYSTEM2007-10-25
K051693 — MODIFICATION TO BAYER ADVIA 2120 HEMATOLOGY ANALYZER WITH AUTOSLIDE SYSTEM2005-12-07
K050235 — IQ 200 URINE ANALYZER BODY FLUIDS MODULE2005-03-23

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.