FDA 510(k)

InnoCare Specialty Foley Catheter

Número K: K241424 · 2024-09-18

Data da decisão2024-09-18

Código do produtoEZL

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

InnoCare Specialty Foley Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Innocare Urologics, LLC. It received FDA 510(k) clearance on 2024-09-18 under 510(k) number K241424. The device is classified under product code EZL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the InnoCare Specialty Foley Catheter?

InnoCare Specialty Foley Catheter is a medical device that received FDA 510(k) clearance on 2024-09-18. The listed applicant is Innocare Urologics, LLC. The 510(k) number is K241424.

When did InnoCare Specialty Foley Catheter receive FDA 510(k) clearance?

InnoCare Specialty Foley Catheter received FDA 510(k) clearance on 2024-09-18, under 510(k) number K241424.

Who is the listed applicant for InnoCare Specialty Foley Catheter?

The FDA 510(k) record lists Innocare Urologics, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for InnoCare Specialty Foley Catheter?

The FDA product code for InnoCare Specialty Foley Catheter is EZL.

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

Dispositivos Relacionados (Código: EZL)

K260756TraumaGuard Intra-Abdominal Pressure-Sensing System (000-0221)Sentinel Medical Technologies,K262056Rusch Latex Gold Foley CatheterTeleflex Medical Sdn. Bhd.K252537Rusch SoftSimplastic Foley CathetersTeleflex Medical Sdn. Bhd.K243011Silicone Urethral Catheter (Silicone Urethral Catheter)Guangdong Ecan Medical Co., Ltd.K232469Rüsch Latex Gold Foley CatheterTeleflexmedical, Inc.K240057TraumaGuard Intra-abdominal Pressure Sensing SystemSentinel Medical Technologies, LLC

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.