FDA 510(k)

The Alma Soprano Titanium

Número K: K230371 · 2023-02-22

Data da decisão2023-02-22

Código do produtoGEX

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

The Alma Soprano Titanium is the device name listed in this FDA 510(k) record. The listed applicant is Alma Lasers, Inc.. It received FDA 510(k) clearance on 2023-02-22 under 510(k) number K230371. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the The Alma Soprano Titanium?

The Alma Soprano Titanium is a medical device that received FDA 510(k) clearance on 2023-02-22. The listed applicant is Alma Lasers, Inc.. The 510(k) number is K230371.

When did The Alma Soprano Titanium receive FDA 510(k) clearance?

The Alma Soprano Titanium received FDA 510(k) clearance on 2023-02-22, under 510(k) number K230371.

Who is the listed applicant for The Alma Soprano Titanium?

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

What is the FDA product code for The Alma Soprano Titanium?

The FDA product code for The Alma Soprano Titanium is GEX. This falls under the Gastroenterology category.

Ensaios clínicos relacionados

Registros relacionados são pareados automaticamente usando nomes, códigos de produtos ou outros metadados. Um pareamento não estabelece um vínculo clínico, científico, corporativo ou regulatório verificado; revise as fontes oficiais vinculadas.

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

Outros registros que listam Alma Lasers, Inc. como candidato(a)

K251684Sistema Alma TED+K250071Sistema de Laser de CO2 Alma FemiLift Pixel, Dispositivos de Entrega e Acessórios K251230The Alma Hybrid Laser System K243044Harmony Alma K233024Harmony Alma K230308Harmony Alma

Ver todos os 14 dispositivos →

Dispositivos Relacionados (Código: GEX)

K254199PicoreMax (PicoreMax)BLUECORE COMPANY Co., Ltd.K252723Dynamis Pro FamilyFotona D.O.O.K241973SmartIPL_NI SystemLumenis Be, Ltd.K261047Dental Diode Laser Device (Laser-Pen)Guilin Kevin Peter Technology Co., Ltd.K261817Diode Laser Therapy System (PZ-BDT67-01, PZ-BDT67-02)Zhengzhou PZ Laser Slim Technology Co., Ltd.K261673LED Therapy Device (QLXY-01)Beijing Nubway S&T Co., Ltd.

Fonte oficial

Ver na base de dados da FDA →

Dados provenientes da FDA Open API. Para informações mais recentes e oficiais, consulte sempre o registro oficial.