Diasorin Liaison CMV Igm/Igg
FDA 510(k) K040290 · Diasorin S.P.A
510(k) numberK040290
Submission
- Device name
- Diasorin Liaison CMV Igm/Igg
- Applicant
- Diasorin S.P.A
Stillwater, MN, US - Received
- February 6, 2004
- Decision date
- June 1, 2005
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- LFZ – Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 866.3175
- Specialty
- Microbiology
Other 510(k)s with product code LFZ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K220949 | Architect CMV IgGLFZ · Traditional | Abbott Laboratories | 10/27/2022SE |
| K220911 | Elecsys CMV IgGLFZ · Traditional | Roche Diagnostics | 10/12/2022SE |
| K181213 | ADVIA Centaur CMV IgG and ADVIA Centaur CMV IgG Quality ControlLFZ · Traditional | Siemens Healthcare Diagnostics, Inc. | 07/30/2018SE |
| K163569 | Elecsys CMV IgMLFZ · Traditional | Roche Diagnostics | 03/17/2017SE |
| K162969 | LIAISON® CMV IgG and LIAISON® CMV IgG Serum Control SetLFZ · Special | DiaSorin, Inc. | 01/06/2017SE |
| K142133 | Elecys CMV Igm Immunoassay; Elecys Precicontrol CMV IgmLFZ · Traditional | Roche Diagnostics | 10/24/2014SE |
| K131605 | Elecsys Precicontrol CMV Igg, Elecsys CMV Igg ImmunoassayLFZ · Traditional | Roche Diagnostics | 02/28/2014SE |
| K993952 | Immulite 2000 CMV Igg, Model L2KCV2, L2KCV6LFZ · Special | Diagnostic Products Corp. | 12/16/1999SE |
| K982485 | Seraquest CMV IgmLFZ · Traditional | Quest Intl., Inc. | 01/13/1999SE |
| K984139 | The Aptus (Automated) Application of the CMV Igg Elisa Test System. an Enzyme Linked…LFZ · Traditional | Zeus Scientific, Inc. | 01/11/1999SE |
More from Zeus Scientific, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K052499 | Diasorin Liaison Toxo Igg and Liaison Toxo Igm AssaysLGD · Traditional | 02/08/2006SE |
Questions and answers
When was Diasorin Liaison CMV Igm/Igg cleared by the FDA?
Diasorin Liaison CMV Igm/Igg (K040290) received a 510(k) decision of Substantially Equivalent on June 1, 2005, 481 days after the submission was received.
What is the product code of K040290?
The FDA product code is LFZ – Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus, a Class II (moderate risk) device regulated under 21 CFR 866.3175.