In Vitro Diagnostic Urine Reagent Strips Set

FDA 510(k) K942648 · Teco Diagnostics

Substantially Equivalent

510(k) numberK942648

Submission

Device name
In Vitro Diagnostic Urine Reagent Strips Set
Applicant
Teco Diagnostics
Placentia, CA, US
Received
June 3, 1994
Decision date
March 24, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

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

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More from Teco Diagnostics

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K170118Scanostics UTI Check Application Test SystemJMT · Traditional 09/21/2017SE
K161527Teco Creatinine Enzymatic Reagent KitJFY · Traditional 07/21/2017SE
K170200Carbon Dioxide Reagent SetKHS · Traditional 06/01/2017SE
K160372Uritek TC-201 Urine Chemistry Test SystemJIL · Traditional 07/22/2016SE
K152835Uritek TC-201 Urine Chemistry Test SystemJFY · Traditional 03/07/2016SE
K141289Tc-Thunderbolt Automated Urine Analyzer System and Tc-Thunderbolt URS-10 StripsJIL · Traditional 07/24/2015SE
K131600URS-2GP (Glucose Protein) Urine StripsJIL · Traditional 05/29/2014SE
K111206Teco Diagnostics Saliva Alcohol TestDIC · Traditional 10/04/2011SE
K100024Teco Diagnostics Uti Detection StripsJMT · Traditional 02/17/2011SE
K101673Uritek TC-101 Urine Analyzer, Urine Reagent Strips 10, Models TC-101, URS-10JIL · Traditional 02/04/2011SE

Questions and answers

When was In Vitro Diagnostic Urine Reagent Strips Set cleared by the FDA?

In Vitro Diagnostic Urine Reagent Strips Set (K942648) received a 510(k) decision of Substantially Equivalent on March 24, 1995, 294 days after the submission was received.

What is the product code of K942648?

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