Corning Certain -Ise

FDA 510(k) K851939 · Corning Medical & Scientific

Substantially Equivalent

510(k) numberK851939

Submission

Device name
Corning Certain -Ise
Applicant
Corning Medical & Scientific
Medfield, MA, US
Received
May 3, 1985
Decision date
June 14, 1985
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 Corning Certain -Ise cleared by the FDA?

Corning Certain -Ise (K851939) received a 510(k) decision of Substantially Equivalent on June 14, 1985, 42 days after the submission was received.

What is the product code of K851939?

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