Doument TM Linearity Test Standards

FDA 510(k) K843947 · Casco Standards

Substantially Equivalent

510(k) numberK843947

Submission

Device name
Doument TM Linearity Test Standards
Applicant
Casco Standards
Yarmouth, ME, US
Received
October 9, 1984
Decision date
October 17, 1984
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 Doument TM Linearity Test Standards cleared by the FDA?

Doument TM Linearity Test Standards (K843947) received a 510(k) decision of Substantially Equivalent on October 17, 1984, 8 days after the submission was received.

What is the product code of K843947?

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