Esensor Cystic Fibrosis Carrier Detection Test , Esensor 4800 DNA Detection System, Model 4800
FDA 510(k) K051435 · Clinical Micro Sensors
Submission
- Device name
- Esensor Cystic Fibrosis Carrier Detection Test , Esensor 4800 DNA Detection System, Model 4800
- Applicant
- Clinical Micro Sensors
Pasadena, CA, US - Received
- June 1, 2005
- Decision date
- January 19, 2006
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- NUA – System, Cystic Fibrosis Transmembrane Conductance Regulator, Gene Mutation Detection
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 866.5900
- Specialty
- Immunology
The cftr gene mutation detection system is a device used to simultaneously detect and identify a panel of mutations and variants in the cftr gene. It is intended as an aid in confirmatory diagnostic testing of individuals with suspected cystic fibrosis (cf), carrier identification, and newborn screening. This device is not intended for stand-alone diagnostic purposes, prenatal diagnostic…
Other 510(k)s with product code NUA
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K163347 | xTAG Cystic Fibrosis 39 Kit v2NUA · Special | Luminex Molecular Diagnostics, Inc. | 12/15/2016SESK |
| K163336 | xTAG Cystic Fibrosis 60 Kit v2, xTAG Data Analysis Software (TDAS) CFTRNUA · Special | Luminex Molecular Diagnostics, Inc. | 12/15/2016SESK |
| K083845 | Xtag CF60 Kit V2NUA · Traditional | Luminex Molecular Diagnostics, Inc. | 12/11/2009SE |
| K083846 | Xtag Cystic Fibrosis 39 Kit V2, (CFTR 39 Kit V2), Model I027C0231, I027D0266, I027E0267NUA · Traditional | Luminex Molecular Diagnostics, Inc. | 09/01/2009SE |
| K083294 | Verigene CFTR Nucleic Acid Test and Verigene CFTR Polyt Nucleic Acid TestNUA · Traditional | Nanosphere, Inc. | 07/24/2009SE |
| K090901 | Esensor CF Genotyping Testm Esensor System, Esensor Cystic Fibrosis Genotyping Test…NUA · Traditional | Osmetech Molecular Diagnostics | 07/06/2009SE |
| K063787 | Inplex CF Molecular TestNUA · Traditional | Third Wave Technologies, Inc. | 03/13/2008SE |
| K062028 | Cystic Fibrosis Genotyping Assay, Model 6L20-01NUA · Traditional | Celera Diagnostics | 09/07/2007SE |
| K060627 | Tag-It Cystic Fibrosis KitNUA · Special | Tm Bioscience Corporation | 06/07/2006SE |
| K060543 | Esensor Cystic Fibrosis Carrier Detection System, Model Esensor 4800NUA · Special | Clinical Micro Sensors, Inc. | 03/28/2006SE |
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Questions and answers
When was Esensor Cystic Fibrosis Carrier Detection Test , Esensor 4800 DNA Detection System, Model 4800 cleared by the FDA?
Esensor Cystic Fibrosis Carrier Detection Test , Esensor 4800 DNA Detection System, Model 4800 (K051435) received a 510(k) decision of Substantially Equivalent on January 19, 2006, 232 days after the submission was received.
What is the product code of K051435?
The FDA product code is NUA – System, Cystic Fibrosis Transmembrane Conductance Regulator, Gene Mutation Detection, a Class II (moderate risk) device regulated under 21 CFR 866.5900.