Mega-Diastix

FDA 510(k) K761310 · Miles Laboratories, Inc.

Substantially Equivalent

510(k) numberK761310

Submission

Device name
Mega-Diastix
Applicant
Miles Laboratories, Inc.
Mchenry, IL, US
Received
December 23, 1976
Decision date
March 21, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JIL – Method, Enzymatic, Glucose (Urinary, Non-Quantitative)
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1340
Specialty
Clinical Chemistry

Other 510(k)s with product code JIL

510(k)DeviceApplicantDecision
K193514AUTION MAX AX-4060 Urinalysis SystemJIL · Traditional Arkray, Inc.04/13/2023SE
K183432cobas u 601 urinalysis test systemJIL · Traditional Roche Diagnostics05/07/2019SE
K173327DIP/U.S. Urine Analysis Test SystemJIL · Traditional Healthy.Io, Ltd.07/18/2018SE
K180356inui In-Home Urine Analysis Test SystemJIL · Traditional Scanadu, Inc.05/25/2018SE
K181024DUS 2GP Reagent Strips, DUS 5 Reagent Strips, DUS 10 Reagent StripsJIL · Traditional DFI Co., Ltd.05/23/2018SE
K171521DUS R-50S (Urine Chemistry system)JIL · Traditional DFI Co., Ltd.02/16/2018SE
K171083iChemVELOCITY Automated Urine Chemistry SystemJIL · Traditional Iris Diagnostics, A Division of Iris…05/12/2017SE
K160062AUTION ELEVEN Semi-Automated Urinalysis SystemJIL · Traditional Arkray, Inc.10/07/2016SE
K160372Uritek TC-201 Urine Chemistry Test SystemJIL · Traditional Teco Diagnostics, Inc.07/22/2016SE
K141289Tc-Thunderbolt Automated Urine Analyzer System and Tc-Thunderbolt URS-10 StripsJIL · Traditional Teco Diagnostics07/24/2015SE

More from Teco Diagnostics

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 Mega-Diastix cleared by the FDA?

Mega-Diastix (K761310) received a 510(k) decision of Substantially Equivalent on March 21, 1977, 88 days after the submission was received.

What is the product code of K761310?

The FDA product code is JIL – Method, Enzymatic, Glucose (Urinary, Non-Quantitative), a Class II (moderate risk) device regulated under 21 CFR 862.1340.