Randox Urinalysis Controls, Levels 1 and 2

FDA 510(k) K110846 · Randox Laboratories Limited

Substantially Equivalent

510(k) numberK110846

Submission

Device name
Randox Urinalysis Controls, Levels 1 and 2
Applicant
Randox Laboratories Limited
Crumlin, GB
Received
March 28, 2011
Decision date
September 30, 2011
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JJW – Urinalysis Controls (Assayed And Unassayed)
Device class
Class I (low risk)
Regulation
21 CFR 862.1660
Specialty
Clinical Chemistry

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Questions and answers

When was Randox Urinalysis Controls, Levels 1 and 2 cleared by the FDA?

Randox Urinalysis Controls, Levels 1 and 2 (K110846) received a 510(k) decision of Substantially Equivalent on September 30, 2011, 186 days after the submission was received.

What is the product code of K110846?

The FDA product code is JJW – Urinalysis Controls (Assayed And Unassayed), a Class I (low risk) device regulated under 21 CFR 862.1660.