Dakocytomation Er/Pr Pharmdx Kit
FDA 510(k) K042884 · Dakocytomation California, Inc.
510(k) numberK042884
Submission
- Device name
- Dakocytomation Er/Pr Pharmdx Kit
- Applicant
- Dakocytomation California, Inc.
Carpinteria, CA, US - Received
- October 19, 2004
- Decision date
- February 15, 2005
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MXZ – Immunohistochemistry Assay, Antibody, Progesterone Receptor
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 864.1860
- Specialty
- Hematology
Other 510(k)s with product code MXZ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K193393 | BOND Ready-to-Use Primary Antibody Progesterone Receptor (16), Novocastra Liquid Mouse…MXZ · Traditional | Leica Biosystems Newcastle, Ltd. | 03/06/2020SE |
| K183102 | BOND Ready-to-Use (RTU) Primary Antibody Progesterone Receptor (16) , Novocastra…MXZ · Special | Leica Biosystems Newcastle, Limited | 12/07/2018SE |
| K170005 | FLEX Monoclonal Mouse Anti-Human Progesterone Receptor, Clone PgR 1294, Ready-to-Use…MXZ · Traditional | Dako Denmark A/S | 12/21/2017SE |
| K171753 | BOND Ready-to-Use (RTU) Primary Antibody Progesterone Receptor (16), Novocastra Liquid…MXZ · Special | Leica Biosystems Newcastle, Limited | 07/21/2017SE |
| K160922 | FLEX Monoclonal Rabbitt Anti-Human Estrogen Receptor a, Clone EP1, Ready-to-Use (Link)…MXZ · Special | Dako North America, Inc. | 05/03/2016SE |
| K130861 | Monoclonal Mouse Anti-Human Progesterone Receptor, Clone PGR 636, Ready-To-Use (Link)MXZ · Traditional | Dako North America, Inc. | 12/09/2013SE |
| K103818 | Confirm Anti-Progestorone Receptor (1E2) Rabbit Monoclonal Primary AntibodyMXZ · Traditional | Ventana Medical Sytems, Inc. | 11/16/2011SE |
| K062615 | Vision Biosystems Progesterone Receptor PGR Clone 16MXZ · Abbreviated | Vision Biosystems, Inc. | 01/29/2007SE |
| K060462 | Neomarkers Rabbit Monoclonal Anti-Human Progesterone Receptor Antibody (Clone SP2)MXZ · Traditional | Lab Vision Corp. | 04/24/2006SE |
| K012960 | Biogenex Monoclonal Anti-Progesterone ReceptorMXZ · Traditional | Biogenex Laboratories | 03/08/2002SE |
More from Biogenex Laboratories
| 510(k) | Device | Decision |
|---|---|---|
| K060423 | Cyan DXD, Multitest CD8/CD4/CD3, CD3-FITC, CD3-RPE, CD3-APC and FluorospheresGKZ · Traditional | 08/15/2006SE |
Questions and answers
When was Dakocytomation Er/Pr Pharmdx Kit cleared by the FDA?
Dakocytomation Er/Pr Pharmdx Kit (K042884) received a 510(k) decision of Substantially Equivalent on February 15, 2005, 119 days after the submission was received.
What is the product code of K042884?
The FDA product code is MXZ – Immunohistochemistry Assay, Antibody, Progesterone Receptor, a Class II (moderate risk) device regulated under 21 CFR 864.1860.