Dakocytomation BETA-2-MICROGLOBULIN Kit, Code No. Oa 368

FDA 510(k) K032692 · Dako A/S

Substantially Equivalent

510(k) numberK032692

Submission

Device name
Dakocytomation BETA-2-MICROGLOBULIN Kit, Code No. Oa 368
Applicant
Dako A/S
Chicago, IL, US
Received
September 2, 2003
Decision date
January 22, 2004
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JZG – System, Test, Beta-2-Microglobulin Immunological
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5630
Specialty
Immunology

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Questions and answers

When was Dakocytomation BETA-2-MICROGLOBULIN Kit, Code No. Oa 368 cleared by the FDA?

Dakocytomation BETA-2-MICROGLOBULIN Kit, Code No. Oa 368 (K032692) received a 510(k) decision of Substantially Equivalent on January 22, 2004, 142 days after the submission was received.

What is the product code of K032692?

The FDA product code is JZG – System, Test, Beta-2-Microglobulin Immunological, a Class II (moderate risk) device regulated under 21 CFR 866.5630.