FDA 510(k)

cobas liat Bordetella panel nucleic acid test

N.º K: K243753 · 2025-11-20

SolicitanteRoche Molecular Systems, Inc.

Fecha de decisión2025-11-20

Código de productoOZZ

Comité asesorMI

DecisiónSubstantially Equivalent

Resumen del dispositivo

cobas liat Bordetella panel nucleic acid test is the device name listed in this FDA 510(k) record. The listed applicant is Roche Molecular Systems, Inc.. It received FDA 510(k) clearance on 2025-11-20 under 510(k) number K243753. The device is classified under product code OZZ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the cobas liat Bordetella panel nucleic acid test?

cobas liat Bordetella panel nucleic acid test is a medical device that received FDA 510(k) clearance on 2025-11-20. The listed applicant is Roche Molecular Systems, Inc.. The 510(k) number is K243753.

When did cobas liat Bordetella panel nucleic acid test receive FDA 510(k) clearance?

cobas liat Bordetella panel nucleic acid test received FDA 510(k) clearance on 2025-11-20, under 510(k) number K243753.

Who is the listed applicant for cobas liat Bordetella panel nucleic acid test?

The FDA 510(k) record lists Roche Molecular Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for cobas liat Bordetella panel nucleic acid test?

The FDA product code for cobas liat Bordetella panel nucleic acid test is OZZ.

Ensayos clínicos relacionados

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Otros registros que enlistan a Roche Molecular Systems, Inc. como solicitante

K260045cobas® Cdiff Nucleic acid test for use on the cobas® Liat® System (07454945190); cobas® Cdiff Positive and Negative Control Kit for use on the cobas® Liat® System (07454970190)K260047cobas Strep A Nucleic acid test for use on the cobas Liat System (07341911190); cobas Strep A Quality Control Kit (07402678190)K260021cobas® BV/CV K260917cobas CT/NG for use on the cobas 5800/6800/8800 systems; cobas TV/MG for use on the cobas 5800/6800/8800 systems K253756cobas liat CT/NG nucleic acid test K253759cobas liat CT/NG/MG nucleic acid test

Ver todos los 36 dispositivos →

Dispositivos relacionados (Código: OZZ)

K183223Simplexa Bordetella Direct, Simplexa Bordetella Positive Control PackDiasorin Molecular, LLC K173498Simplexa Bordetella Direct, Simplexa Bordetella Positive Control PackDiasorin Molecular, LLC K181029Solana Bordetella Complete AssayQuidel Corporation K163626ARIES Bordetella Assay; ARIES Bordetella Assay Protocol File KitLuminex Corporation K170284Great Basin Bordetella Direct TestGreat Basin Scientific, Inc.

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.