Dimension Whole Blood Cholesterol

FDA 510(k) K880723 · Technimed, Inc.

Substantially Equivalent

510(k) numberK880723

Submission

Device name
Dimension Whole Blood Cholesterol
Applicant
Technimed, Inc.
Fort Lauderdale, FL, US
Received
February 23, 1988
Decision date
November 8, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CHH – Enzymatic Esterase--Oxidase, Cholesterol
Device class
Class I (low risk)
Regulation
21 CFR 862.1175
Specialty
Clinical Chemistry

Other 510(k)s with product code CHH

510(k)DeviceApplicantDecision
K251091LipidsCHH · Traditional Truvian Health12/30/2025SE
K232404CHOLESTEROL; HDL-cholesterol ; LDL-cholesterol; TRIGLYCERIDESCHH · Traditional Medicon Hellas S.A08/09/2024SE
K203597Cholesterol2CHH · Traditional Abbott Ireland Diagnostics Division06/30/2022SE
K190490VITROS XT Chemistry Products TRIG-CHOL SlidesCHH · Traditional Ortho-Clinical Diagnostics, Inc.03/27/2019SE
K181373Extended Lipid Panel AssayCHH · Traditional Laboratory Corporation of America Holdings10/18/2018SE
K180504Mission Lipid Panel Monitoring SystemCHH · Special ACON Laboratories, Inc.03/28/2018SE
K163406Mission Cholesterol Monitoring System, Mission Cholesterol Pro Monitoring SystemCHH · Traditional ACON Laboratories, Inc.07/11/2017SE
K151545CardioChek Plus Test System, CardioChek Home Test System, CardioChek PA Test System…CHH · Traditional Polymer Technology Systems, Inc.12/22/2016SE
K150654CholesterolCHH · Traditional Randox Laboratories, Ltd.09/29/2015SE
K132031Afinion Lipid Panel and Afinion Lipid Panel ControlCHH · Traditional Axis-Shield Poc AS03/21/2014SE

Questions and answers

When was Dimension Whole Blood Cholesterol cleared by the FDA?

Dimension Whole Blood Cholesterol (K880723) received a 510(k) decision of Substantially Equivalent on November 8, 1988, 259 days after the submission was received.

What is the product code of K880723?

The FDA product code is CHH – Enzymatic Esterase--Oxidase, Cholesterol, a Class I (low risk) device regulated under 21 CFR 862.1175.