Teco Ise Reagent Set for CX System

FDA 510(k) K052724 · Teco Diagnostics

Substantially Equivalent

510(k) numberK052724

Submission

Device name
Teco Ise Reagent Set for CX System
Applicant
Teco Diagnostics
Anaheim, CA, US
Received
September 29, 2005
Decision date
December 14, 2005
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JGS – Electrode, Ion Specific, Sodium
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1665
Specialty
Clinical Chemistry

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Questions and answers

When was Teco Ise Reagent Set for CX System cleared by the FDA?

Teco Ise Reagent Set for CX System (K052724) received a 510(k) decision of Substantially Equivalent on December 14, 2005, 76 days after the submission was received.

What is the product code of K052724?

The FDA product code is JGS – Electrode, Ion Specific, Sodium, a Class II (moderate risk) device regulated under 21 CFR 862.1665.