Dri-Stat Enzymatic Bilirubin Test Kit

FDA 510(k) K843174 · Beckman Instruments, Inc.

Substantially Equivalent

510(k) numberK843174

Submission

Device name
Dri-Stat Enzymatic Bilirubin Test Kit
Applicant
Beckman Instruments, Inc.
Mchenry, IL, US
Received
August 13, 1984
Decision date
September 14, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JFM – Enzymatic Method, Bilirubin
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1110
Specialty
Clinical Chemistry

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Questions and answers

When was Dri-Stat Enzymatic Bilirubin Test Kit cleared by the FDA?

Dri-Stat Enzymatic Bilirubin Test Kit (K843174) received a 510(k) decision of Substantially Equivalent on September 14, 1984, 32 days after the submission was received.

What is the product code of K843174?

The FDA product code is JFM – Enzymatic Method, Bilirubin, a Class II (moderate risk) device regulated under 21 CFR 862.1110.