Captia HSV 2 Igg Type Specific Elisa Kit
FDA 510(k) K033106 · Trinity Biotech USA
510(k) numberK033106
Submission
- Device name
- Captia HSV 2 Igg Type Specific Elisa Kit
- Applicant
- Trinity Biotech USA
Jamestown, NY, US - Received
- September 30, 2003
- Decision date
- July 13, 2004
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary 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
Other 510(k)s with product code MYF
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| 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 |
| K061239 | Euroimmun ANTI-HSV-2 Elisa (Igg) and ANTI-HSV-1 Elisa (Igg) KitMYF · Traditional | Euroimmun Us, LLC | 06/28/2007SE |
| K993724 | HSV-2 Elisa Igg, Model EL0920GMYF · Traditional | Mrl Diagnostics | 02/01/2000SE |
More from Mrl Diagnostics
| 510(k) | Device | Decision |
|---|---|---|
| K140455 | Captia Measles IgmPCL · Traditional | 05/22/2014SE |
| K033105 | Captia HSV 1 Igg Type Specific Elisa KitMXJ · Traditional | 07/13/2004SE |
| K033083 | Borrelia Burgdorferi Igg/Igm Elisa Test SystemLSR · Traditional | 11/26/2003SE |
| K033079 | Chlamydia Igg Elisa Test SystemLJC · Traditional | 11/26/2003SE |
| K033070 | Borrelia Burgdorferi Igm Elisa Test SystemLSR · Traditional | 11/26/2003SE |
| K033067 | Pylori IggLYR · Traditional | 11/26/2003SE |
| K033064 | Mycoplasma IggLON · Traditional | 11/26/2003SE |
| K033051 | Legionella Pneumophila Igg/IgmMJH · Traditional | 11/26/2003SE |
| K993839 | Ena Profile Elisa Test SystemLLL · Traditional | 01/12/2000SE |
| K992665 | Macra Lp(A) Enzyme Immunoassay KitDFC · Traditional | 11/26/1999SE |
Questions and answers
When was Captia HSV 2 Igg Type Specific Elisa Kit cleared by the FDA?
Captia HSV 2 Igg Type Specific Elisa Kit (K033106) received a 510(k) decision of Substantially Equivalent on July 13, 2004, 287 days after the submission was received.
What is the product code of K033106?
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.