FDA 510(k)

STAR 65

N.º K: K172147 · 2018-05-25

SolicitanteSkanray Technologies Pvt, Ltd.

Fecha de decisión2018-05-25

Código de productoMWI

Comité asesorCV

DecisiónSubstantially Equivalent

Resumen del dispositivo

STAR 65 is the device name listed in this FDA 510(k) record. The listed applicant is Skanray Technologies Pvt, Ltd.. It received FDA 510(k) clearance on 2018-05-25 under 510(k) number K172147. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the STAR 65?

STAR 65 is a medical device that received FDA 510(k) clearance on 2018-05-25. The listed applicant is Skanray Technologies Pvt, Ltd.. The 510(k) number is K172147.

When did STAR 65 receive FDA 510(k) clearance?

STAR 65 received FDA 510(k) clearance on 2018-05-25, under 510(k) number K172147.

Who is the listed applicant for STAR 65?

The FDA 510(k) record lists Skanray Technologies Pvt, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STAR 65?

The FDA product code for STAR 65 is MWI.

Dispositivos relacionados (Código: MWI)

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.

K260438Vital Signs Monitor (CLEO2)Infinium Medical, Inc.K253417Masimo Root Monitoring SystemMasimo Corporation K253196Midmark 800 Digital Vital Signs Device (1-300-0100, 1-300-0200, 1-300-0300, 1-300-0400)Midmark Corporation K253436c-med0 alphaCosinuss GmbH K250135WAVE Clinical Platform (2.0.000)Baxter Healthcare Corp/ Excel Medical K241766QMAPP® (Hemo, Hemo Lite, PCM, GO, Hybrid)Fysicon BV

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.