Euroimmun ANTI-HSV-2 Elisa (Igg) and ANTI-HSV-1 Elisa (Igg) Kit
FDA 510(k) K061239 · Euroimmun Us, LLC
510(k) numberK061239
Submission
- Device name
- Euroimmun ANTI-HSV-2 Elisa (Igg) and ANTI-HSV-1 Elisa (Igg) Kit
- Applicant
- Euroimmun Us, LLC
Boonton Township, NJ, US - Received
- May 3, 2006
- Decision date
- June 28, 2007
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- MYF – Enzyme Linked Immunosorbent Assay, Herpes Simplex Virus, Hsv-2
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 866.3305
- Specialty
- Microbiology
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|---|---|---|---|
| K243575 | ARCHITECT HSV-2 IgG, ARCHITECT HSV-2 IgG Calibrator, ARCHITECT HSV-2 IgG ControlsMYF · Traditional | Biokit, S.A. | 02/12/2025SE |
| K220924 | Elecsys HSV-2 IgG (08948887160)MYF · Traditional | Roche Diagnostics | 10/12/2022SE |
| K181514 | SeraQuest HSV Type 2 Specific IgGMYF · Traditional | Quest International, Inc. | 06/13/2019SE |
| K181334 | ADVIA Centaur Herpes-2 IgGMYF · Traditional | Biokit, S.A. | 08/23/2018SE |
| K152353 | SeraQuest HSV Type 2 Specific IgGMYF · Traditional | Quest International, Inc. | 05/13/2016SE |
| K103603 | Zeus Elisa HSV GG-2 Igg Test SystemMYF · Traditional | Zeus Scientific, Inc. | 05/20/2011SE |
| K081687 | Liaison HSV-2 Type Specific Igg Assay, Control HSV-2 IggMYF · Traditional | DiaSorin, Inc. | 11/10/2008SE |
| K033106 | Captia HSV 2 Igg Type Specific Elisa KitMYF · Traditional | Trinity Biotech USA | 07/13/2004SE |
| K993724 | HSV-2 Elisa Igg, Model EL0920GMYF · Traditional | Mrl Diagnostics | 02/01/2000SE |
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Questions and answers
When was Euroimmun ANTI-HSV-2 Elisa (Igg) and ANTI-HSV-1 Elisa (Igg) Kit cleared by the FDA?
Euroimmun ANTI-HSV-2 Elisa (Igg) and ANTI-HSV-1 Elisa (Igg) Kit (K061239) received a 510(k) decision of Substantially Equivalent on June 28, 2007, 421 days after the submission was received.
What is the product code of K061239?
The FDA product code is MYF – Enzyme Linked Immunosorbent Assay, Herpes Simplex Virus, Hsv-2, a Class II (moderate risk) device regulated under 21 CFR 866.3305.