Phoenix Electrolyte Calibration Set for the Dade/Behring/Behring Dimension Chemistry System

FDA 510(k) K012509 · Phoenix Diagnostics, Inc.

Substantially Equivalent

510(k) numberK012509

Submission

Device name
Phoenix Electrolyte Calibration Set for the Dade/Behring/Behring Dimension Chemistry System
Applicant
Phoenix Diagnostics, Inc.
Natick, MA, US
Received
August 6, 2001
Decision date
October 9, 2001
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JIX – Calibrator, Multi-Analyte Mixture
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1150
Specialty
Clinical Chemistry

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Questions and answers

When was Phoenix Electrolyte Calibration Set for the Dade/Behring/Behring Dimension Chemistry System cleared by the FDA?

Phoenix Electrolyte Calibration Set for the Dade/Behring/Behring Dimension Chemistry System (K012509) received a 510(k) decision of Substantially Equivalent on October 9, 2001, 64 days after the submission was received.

What is the product code of K012509?

The FDA product code is JIX – Calibrator, Multi-Analyte Mixture, a Class II (moderate risk) device regulated under 21 CFR 862.1150.