Wako Lipid Control, Level 1 and Level 2

FDA 510(k) K040918 · Wako Chemicals USA, Inc.

Substantially Equivalent

510(k) numberK040918

Submission

Device name
Wako Lipid Control, Level 1 and Level 2
Applicant
Wako Chemicals USA, Inc.
Richmond, VA, US
Received
April 8, 2004
Decision date
May 17, 2004
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JJX – Single (Specified) Analyte 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 Wako Lipid Control, Level 1 and Level 2 cleared by the FDA?

Wako Lipid Control, Level 1 and Level 2 (K040918) received a 510(k) decision of Substantially Equivalent on May 17, 2004, 39 days after the submission was received.

What is the product code of K040918?

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