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.

FDA 510(k)

HyperView Hyperspectral Tissue Oxygenation Measurement System

N.º K: K161237 · 2016-12-16

SolicitanteHypermed Imaging, Inc.
Fecha de decisión2016-12-16
Código de productoMUD
Comité asesorCV
DecisiónSubstantially Equivalent

Resumen del dispositivo

HyperView Hyperspectral Tissue Oxygenation Measurement System is the device name listed in this FDA 510(k) record. The listed applicant is Hypermed Imaging, Inc.. It received FDA 510(k) clearance on 2016-12-16 under 510(k) number K161237. The device is classified under product code MUD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the HyperView Hyperspectral Tissue Oxygenation Measurement System?

HyperView Hyperspectral Tissue Oxygenation Measurement System is a medical device that received FDA 510(k) clearance on 2016-12-16. The listed applicant is Hypermed Imaging, Inc.. The 510(k) number is K161237.

When did HyperView Hyperspectral Tissue Oxygenation Measurement System receive FDA 510(k) clearance?

HyperView Hyperspectral Tissue Oxygenation Measurement System received FDA 510(k) clearance on 2016-12-16, under 510(k) number K161237.

Who is the listed applicant for HyperView Hyperspectral Tissue Oxygenation Measurement System?

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

What is the FDA product code for HyperView Hyperspectral Tissue Oxygenation Measurement System?

The FDA product code for HyperView Hyperspectral Tissue Oxygenation Measurement System is MUD.

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

Dispositivos relacionados (Código: MUD)

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.

K254129Spectrum-2Neko Health ABK243324Masimo O3 Regional OximeterMasimo CorporationK250519Lap.Ox™ Laparoscopic Tissue OximeterViOptix, Inc.K240596Algoritmo de Índice de Autoregulación Cerebral (CAI)Edwards LifesciencesK241393ODI-TechOdi Medical ASK240601SnapshotNIR model KD205Kent Imaging, 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.

↑