Roche Cobas Amplicor Chlamydia Trachomatis Test
FDA 510(k) K964507 · Roche Molecular Systems, Inc.
510(k) numberK964507
Submission
- Device name
- Roche Cobas Amplicor Chlamydia Trachomatis Test
- Applicant
- Roche Molecular Systems, Inc.
Branchburg, NJ, US - Received
- November 8, 1996
- Decision date
- June 13, 1997
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MKZ – Dna Probe, Nucleic Acid Amplification, Chlamydia
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 866.3120
- Specialty
- Microbiology
Other 510(k)s with product code MKZ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K230451 | Aptima® Chlamydia trachomatis AssayMKZ · Traditional | Hologic, Inc. | 11/16/2023SE |
| K140446 | BD Probetec Chlamydia Trachomatis (CT) QX Amplified DNA AssayMKZ · Traditional | Becton, Dickinson & CO | 05/20/2014SE |
| K110923 | Cobas 4800 CT / NG TestMKZ · Traditional | Roche Molecular Systems, Inc. | 01/24/2012SE |
| K091724 | BD Probetec Chlamydia Trachomatis (CT) Q Amplified DNA AssayMKZ · Traditional | Becton, Dickinson & CO | 11/13/2009SE |
| K090824 | BD Probetec Chlamydia Trachomatis (CT) QX Amplified DNA AssayMKZ · Traditional | Becton, Dickinson & CO | 06/02/2009SE |
| K081824 | BD Probetec Chlamydia Trachomatis (CT) Q Amplified DNA AssayMKZ · Traditional | Becton, Dickinson & CO | 12/11/2008SE |
| K080739 | Abbott Realtime Ct/Ng Assay and Multi-Collect Specimen Collection KitMKZ · Traditional | Abbott Molecular, Inc. | 07/10/2008SE |
| K070174 | Amplicor Ct/Ng Test for Chlamydia Trachomatis; Roche Scripts for Ct/Ng Test AccessoryMKZ · Traditional | Roche Diagnostics Corporation | 04/16/2007SE |
| K063451 | Gen-Probe Aptima Assay for Chlamydia Trachomatis, Model 1199MKZ · Traditional | Gen-Probe, Inc. | 01/22/2007SE |
| K061413 | Aptima CT Assay on the Tigris DTS SystemMKZ · Traditional | Gen-Probe, Inc. | 10/13/2006SE |
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| K260045 | cobas® Cdiff Nucleic acid test for use on the cobas® Liat® System (07454945190); cobas®…OZN · Traditional | 08/28/2026SE |
| K260021 | cobas® BV/CVPQA · Traditional | 07/16/2026SE |
| K260917 | cobas CT/NG for use on the cobas 5800/6800/8800 systems; cobas TV/MG for use on the…QEP · Traditional | 07/08/2026SE |
| K253759 | cobas liat CT/NG/MG nucleic acid testQEP · Dual Track | 05/15/2026SE |
| K253756 | cobas liat CT/NG nucleic acid testQEP · Dual Track | 05/15/2026SE |
| K243753 | cobas liat Bordetella panel nucleic acid testOZZ · Dual Track | 11/20/2025SE |
| K252484 | cobas HCVMZP · Traditional | 11/03/2025SE |
| K252481 | cobas CMVPAB · Traditional | 11/03/2025SE |
| K243455 | cobas Respiratory 4-flex for use on the cobas 5800/6800/8800 SystemsQOF · Traditional | 07/31/2025SE |
Questions and answers
When was Roche Cobas Amplicor Chlamydia Trachomatis Test cleared by the FDA?
Roche Cobas Amplicor Chlamydia Trachomatis Test (K964507) received a 510(k) decision of Substantially Equivalent on June 13, 1997, 217 days after the submission was received.
What is the product code of K964507?
The FDA product code is MKZ – Dna Probe, Nucleic Acid Amplification, Chlamydia, a Class I (low risk) device regulated under 21 CFR 866.3120.