FDA 510(k)

iQMR

N.º K: K173605 · 2018-03-08

SolicitanteMedic Vision - Imaging Solutions, Ltd.

Fecha de decisión2018-03-08

Código de productoLLZ

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

iQMR is the device name listed in this FDA 510(k) record. The listed applicant is Medic Vision - Imaging Solutions, Ltd.. It received FDA 510(k) clearance on 2018-03-08 under 510(k) number K173605. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the iQMR?

iQMR is a medical device that received FDA 510(k) clearance on 2018-03-08. The listed applicant is Medic Vision - Imaging Solutions, Ltd.. The 510(k) number is K173605.

When did iQMR receive FDA 510(k) clearance?

iQMR received FDA 510(k) clearance on 2018-03-08, under 510(k) number K173605.

Who is the listed applicant for iQMR?

The FDA 510(k) record lists Medic Vision - Imaging Solutions, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for iQMR?

The FDA product code for iQMR is LLZ.

Dispositivos relacionados (Código: LLZ)

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.

K261874Syneris PACS v.1.0.1.0Syneris K262442HipStudio AnalysisReplasia BV K261855Elucid PlaqueIQElucid Bioimaging, Inc.K254214OOOPDSTaiwan Main Orthopaedic Biotechnology Co., Ltd.K261861SPINEsim v1.0Mdsim S.A.K2620603D-RD-SRadiopharmaceutical Imaging & Dosimetry, LLC

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.