N Lp(A) Control Sy

FDA 510(k) K013130 · Dade Behring, Inc.

Substantially Equivalent

510(k) numberK013130

Submission

Device name
N Lp(A) Control Sy
Applicant
Dade Behring, Inc.
Newark, DE, US
Received
September 19, 2001
Decision date
October 18, 2001
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary 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 N Lp(A) Control Sy cleared by the FDA?

N Lp(A) Control Sy (K013130) received a 510(k) decision of Substantially Equivalent on October 18, 2001, 29 days after the submission was received.

What is the product code of K013130?

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.