FDA 510(k)

Voyant Maryland Fusion Device

N.º K: K200598 · 2020-04-08

SolicitanteApplied Medical Resources Corp.

Fecha de decisión2020-04-08

Código de productoGEI

Comité asesorSU

DecisiónSubstantially Equivalent

Resumen del dispositivo

Voyant Maryland Fusion Device is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Resources Corp.. It received FDA 510(k) clearance on 2020-04-08 under 510(k) number K200598. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Voyant Maryland Fusion Device?

Voyant Maryland Fusion Device is a medical device that received FDA 510(k) clearance on 2020-04-08. The listed applicant is Applied Medical Resources Corp.. The 510(k) number is K200598.

When did Voyant Maryland Fusion Device receive FDA 510(k) clearance?

Voyant Maryland Fusion Device received FDA 510(k) clearance on 2020-04-08, under 510(k) number K200598.

Who is the listed applicant for Voyant Maryland Fusion Device?

The FDA 510(k) record lists Applied Medical Resources Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Voyant Maryland Fusion Device?

The FDA product code for Voyant Maryland Fusion Device is GEI.

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 Applied Medical Resources Corp. como solicitante

K252740Voyant® Open Fusion Device (EB240/Open Fusion)K252442Kii Structural Balloon Access System K243152GelPOINT V-Path Transvaginal Access Platform with Retroperitoneal Access Device K201212Voyant Open Fusion Device K193292Voyant 5mm Fusion Device, Voyant Maryland Fusion Device K191294Transvaginal Access Platform

Ver todos los 11 dispositivos →

Dispositivos relacionados (Código: GEI)

K254196HARMONIC 1100 Shears (HAR1120); HARMONIC 1100 Shears (HAR1136)Ethicon Endo-Surgery, LLC K261959Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Push Button Switch (0703-046-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Push Button Switch, Bulk Non-Sterile (0703-046-102);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Rocker Switch (0703-047-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Rocker Switch, Bulk Non-Sterile (0703-047-102)Stryker Instruments K261070LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coatedCovidien, LLC K254185Potenza PrimeJeisys Medical Incorporated K262364Ellian Enigma RF DeviceEllian Corp K253859Scarlet Pro (Scarlet Pro)VIOL Co., Ltd.

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.