Immulite 2000 CMV Igg, Model L2KCV2, L2KCV6

FDA 510(k) K993952 · Diagnostic Products Corp.

Substantially Equivalent

510(k) numberK993952

Submission

Device name
Immulite 2000 CMV Igg, Model L2KCV2, L2KCV6
Applicant
Diagnostic Products Corp.
Los Angeles, CA, US
Received
November 22, 1999
Decision date
December 16, 1999
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LFZ – Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus
Device class
Class II (moderate risk)
Regulation
21 CFR 866.3175
Specialty
Microbiology

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K131605Elecsys Precicontrol CMV Igg, Elecsys CMV Igg ImmunoassayLFZ · Traditional Roche Diagnostics02/28/2014SE
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K032881Immulite/Immulite 1000 Total Testosterone and Immulite 2000 Total TestosteroneCDZ · Special 10/10/2003SE
K023152Immulite 2000 Allergen-Specific IgeDHB · Abbreviated 12/17/2002SE
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Questions and answers

When was Immulite 2000 CMV Igg, Model L2KCV2, L2KCV6 cleared by the FDA?

Immulite 2000 CMV Igg, Model L2KCV2, L2KCV6 (K993952) received a 510(k) decision of Substantially Equivalent on December 16, 1999, 24 days after the submission was received.

What is the product code of K993952?

The FDA product code is LFZ – Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus, a Class II (moderate risk) device regulated under 21 CFR 866.3175.