Immulite CMV Igg

FDA 510(k) K950672 · Diagnostic Products Corp.

Substantially Equivalent

510(k) numberK950672

Submission

Device name
Immulite CMV Igg
Applicant
Diagnostic Products Corp.
Los Angeles, CA, US
Received
February 13, 1995
Decision date
June 17, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 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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K142133Elecys CMV Igm Immunoassay; Elecys Precicontrol CMV IgmLFZ · Traditional Roche Diagnostics10/24/2014SE
K131605Elecsys Precicontrol CMV Igg, Elecsys CMV Igg ImmunoassayLFZ · Traditional Roche Diagnostics02/28/2014SE
K040290Diasorin Liaison CMV Igm/IggLFZ · Traditional Diasorin S.P.A06/01/2005SE
K993952Immulite 2000 CMV Igg, Model L2KCV2, L2KCV6LFZ · Special Diagnostic Products Corp.12/16/1999SE
K982485Seraquest CMV IgmLFZ · Traditional Quest Intl., Inc.01/13/1999SE

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Questions and answers

When was Immulite CMV Igg cleared by the FDA?

Immulite CMV Igg (K950672) received a 510(k) decision of Substantially Equivalent on June 17, 1996, 490 days after the submission was received.

What is the product code of K950672?

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