FDA 510(k)

The Family of UltraPulse CO2 Surgical and Aesthetic Lasers, Delivery Devices and Accessories

Número K: K220467 · 2022-05-18

Data da decisão2022-05-18

Código do produtoGEX

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

The Family of UltraPulse CO2 Surgical and Aesthetic Lasers, Delivery Devices and Accessories is the device name listed in this FDA 510(k) record. The listed applicant is Lumenis Be, Ltd.. It received FDA 510(k) clearance on 2022-05-18 under 510(k) number K220467. 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 Family of UltraPulse CO2 Surgical and Aesthetic Lasers, Delivery Devices and Accessories?

The Family of UltraPulse CO2 Surgical and Aesthetic Lasers, Delivery Devices and Accessories is a medical device that received FDA 510(k) clearance on 2022-05-18. The listed applicant is Lumenis Be, Ltd.. The 510(k) number is K220467.

When did The Family of UltraPulse CO2 Surgical and Aesthetic Lasers, Delivery Devices and Accessories receive FDA 510(k) clearance?

The Family of UltraPulse CO2 Surgical and Aesthetic Lasers, Delivery Devices and Accessories received FDA 510(k) clearance on 2022-05-18, under 510(k) number K220467.

Who is the listed applicant for The Family of UltraPulse CO2 Surgical and Aesthetic Lasers, Delivery Devices and Accessories?

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

What is the FDA product code for The Family of UltraPulse CO2 Surgical and Aesthetic Lasers, Delivery Devices and Accessories?

The FDA product code for The Family of UltraPulse CO2 Surgical and Aesthetic Lasers, Delivery Devices and Accessories 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 Lumenis Be, Ltd. como candidato(a)

K241973SmartIPL_NI System K253803MILAN System K250809Stellar M22 K242349FoLix K233301ULTRApulse Alpha CO2 Laser System, Delivery Devices and Accessories K222790F65 Laser System

Ver todos os 7 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.