Aviso: Este sitio agrega datos públicos oficiales de la FDA, ClinicalTrials.gov, PubMed y SEC EDGAR solo como referencia general. No constituye asesoramiento médico, diagnóstico, recomendaciones de tratamiento ni asesoramiento de inversión.

PMA de la FDA

Tissue adhesive for internal use

Número de PMA: P130023 · 2017-07-27

SolicitanteCohera Medical, Inc.
Fecha de decisión2017-07-27
Número PMAP130023
Código de productoPJK
Clase del dispositivoClase 3
Especialidad médicaG
Número de regulación21 CFR 8
Comité asesorSU

Resumen del dispositivo

Tissue adhesive for internal use is the device name listed in this FDA 510(k) record. The listed applicant is Cohera Medical, Inc.. It received FDA 510(k) clearance on 2017-07-27. The device is classified under product code PJK. It was reviewed by the SU advisory panel.

Preguntas frecuentes

What is the Tissue adhesive for internal use?

Tissue adhesive for internal use is a medical device that received FDA 510(k) clearance on 2017-07-27. The listed applicant is Cohera Medical, Inc..

When did Tissue adhesive for internal use receive FDA 510(k) clearance?

The clearance date for Tissue adhesive for internal use can be found in the official FDA records.

Who is the listed applicant for Tissue adhesive for internal use?

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

What is the FDA product code for Tissue adhesive for internal use?

The FDA product code for Tissue adhesive for internal use is PJK.

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_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

↑