Seralyzer

FDA 510(k) K812100 · Miles Laboratories, Inc.

Substantially Equivalent

510(k) numberK812100

Submission

Device name
Seralyzer
Applicant
Miles Laboratories, Inc.
Mchenry, IL, US
Received
July 24, 1981
Decision date
August 12, 1981
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

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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

More from Axis-Shield Poc AS

510(k)DeviceDecision
K880605Labeling Change for Cutter Pureflo Plus IV FilterFPB · Traditional 05/26/1988SE
K874909Micro-Bumintest Reagent TabletsJIR · Traditional 04/28/1988SE
K875079Modified Seralyzer Alt/Sgpt Reag. Strips & ModuleCKA · Traditional 04/05/1988SE
K871835Glucometer QC Blood Meter, Ames Gluco System PrintCGA · Traditional 12/22/1987SE
K872120Seralyzer III Blood Chemistry AnalyzerJJF · Traditional 10/28/1987SE
K873304Clinitek Auto 2000 Reagent Cassette (Leukocytes)LJX · Traditional 09/11/1987SE
K872634Cutter Pureflo Plus IV FilterFPB · Traditional 08/04/1987SE
K870214Modified Saltex Reagent StripsCHK · Traditional 06/29/1987SE
K870752Seralyzer Ldh/Total Bilirubin/Triglycerides StripsCFJ · Traditional 04/14/1987SE
K865053Sera-Tek Microsomal Antibody TestJZO · Traditional 02/18/1987SE

Questions and answers

When was Seralyzer cleared by the FDA?

Seralyzer (K812100) received a 510(k) decision of Substantially Equivalent on August 12, 1981, 19 days after the submission was received.

What is the product code of K812100?

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