Sera-Tek Microsomal Antibody Test

FDA 510(k) K865053 · Miles Laboratories, Inc.

Substantially Equivalent

510(k) numberK865053

Submission

Device name
Sera-Tek Microsomal Antibody Test
Applicant
Miles Laboratories, Inc.
Elkhart, IN, US
Received
December 24, 1986
Decision date
February 18, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JZO – System, Test, Thyroid Autoantibody
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5870
Specialty
Immunology

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K151799EliA anti-TG Immunoassay, EliA anti-TPO Immunoassay, EliA Thyroid Positive Control 250…JZO · Traditional Phadia AB03/25/2016SE
K152061IMMULITE 2000 TSI Assay, IMMULITE 2000 TSI Calibration Verification MaterialJZO · Traditional Siemens Healthcare Diagnostics, Inc.03/03/2016SE
K092229Thyretain TM Tsi Reporter BioassayJZO · Traditional Diagnostic Hybrids, Inc.05/18/2010SE
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More from Diagnostic Hybrids, Inc.

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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
K864530Seralyzer Glucose (HK) Reagent Strips,Module,Cali.CGA · Traditional 02/18/1987SE

Questions and answers

When was Sera-Tek Microsomal Antibody Test cleared by the FDA?

Sera-Tek Microsomal Antibody Test (K865053) received a 510(k) decision of Substantially Equivalent on February 18, 1987, 56 days after the submission was received.

What is the product code of K865053?

The FDA product code is JZO – System, Test, Thyroid Autoantibody, a Class II (moderate risk) device regulated under 21 CFR 866.5870.