Il Phoenix, Model 900, Chemistry/Electrolyte Analy

FDA 510(k) K884771 · Instrumentation Laboratory CO

Substantially Equivalent

510(k) numberK884771

Submission

Device name
Il Phoenix, Model 900, Chemistry/Electrolyte Analy
Applicant
Instrumentation Laboratory CO
Lexington, MA, US
Received
November 14, 1988
Decision date
February 10, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JFP – Electrode, Ion Specific, Calcium
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1145
Specialty
Clinical Chemistry

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Questions and answers

When was Il Phoenix, Model 900, Chemistry/Electrolyte Analy cleared by the FDA?

Il Phoenix, Model 900, Chemistry/Electrolyte Analy (K884771) received a 510(k) decision of Substantially Equivalent on February 10, 1989, 88 days after the submission was received.

What is the product code of K884771?

The FDA product code is JFP – Electrode, Ion Specific, Calcium, a Class II (moderate risk) device regulated under 21 CFR 862.1145.