Paramax Urine/Csf Calibrator Level I and II

FDA 510(k) K903913 · Baxter Healthcare Corp

Substantially Equivalent

510(k) numberK903913

Submission

Device name
Paramax Urine/Csf Calibrator Level I and II
Applicant
Baxter Healthcare Corp
Santa Ana, CA, US
Received
August 24, 1990
Decision date
September 27, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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 Paramax Urine/Csf Calibrator Level I and II cleared by the FDA?

Paramax Urine/Csf Calibrator Level I and II (K903913) received a 510(k) decision of Substantially Equivalent on September 27, 1990, 34 days after the submission was received.

What is the product code of K903913?

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