Immulite 2500 Vitamin B12 Model L5KVB2-200 TEST,L5KVB6-600 Test, Immulite 2500 Folic Acid Model L5KFO2-200 TEST,L5KFO6-6

FDA 510(k) K060929 · Diagnostic Products Corporation

Substantially Equivalent

510(k) numberK060929

Submission

Device name
Immulite 2500 Vitamin B12 Model L5KVB2-200 TEST,L5KVB6-600 Test, Immulite 2500 Folic Acid Model L5KFO2-200 TEST,L5KFO6-6
Applicant
Diagnostic Products Corporation
Los Angeles, CA, US
Received
April 5, 2006
Decision date
April 28, 2006
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CDD – Radioassay, Vitamin B12
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1810
Specialty
Clinical Chemistry

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Questions and answers

When was Immulite 2500 Vitamin B12 Model L5KVB2-200 TEST,L5KVB6-600 Test, Immulite 2500 Folic Acid Model L5KFO2-200 TEST,L5KFO6-6 cleared by the FDA?

Immulite 2500 Vitamin B12 Model L5KVB2-200 TEST,L5KVB6-600 Test, Immulite 2500 Folic Acid Model L5KFO2-200 TEST,L5KFO6-6 (K060929) received a 510(k) decision of Substantially Equivalent on April 28, 2006, 23 days after the submission was received.

What is the product code of K060929?

The FDA product code is CDD – Radioassay, Vitamin B12, a Class II (moderate risk) device regulated under 21 CFR 862.1810.