Affinity HLH Test System

FDA 510(k) K903407 · Bd Becton Dickinson Vacutainer Systems Preanalytic

Substantially Equivalent

510(k) numberK903407

Submission

Device name
Affinity HLH Test System
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic
Franklin Lakes, NJ, US
Received
July 31, 1990
Decision date
September 7, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JJY – Multi-Analyte Controls, All Kinds (Assayed)
Device class
Class I (low risk)
Regulation
21 CFR 862.1660
Specialty
Clinical Chemistry

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Questions and answers

When was Affinity HLH Test System cleared by the FDA?

Affinity HLH Test System (K903407) received a 510(k) decision of Substantially Equivalent on September 7, 1990, 38 days after the submission was received.

What is the product code of K903407?

The FDA product code is JJY – Multi-Analyte Controls, All Kinds (Assayed), a Class I (low risk) device regulated under 21 CFR 862.1660.