FDA 510(k)

Natural Rubber Latex Ultrasound Transducer Probe Covers

Número K: K213087 · 2022-06-07

Data da decisão2022-06-07

Código do produtoITX

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do dispositivo

Natural Rubber Latex Ultrasound Transducer Probe Covers is the device name listed in this FDA 510(k) record. The listed applicant is Global Protection Corp.. It received FDA 510(k) clearance on 2022-06-07 under 510(k) number K213087. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Natural Rubber Latex Ultrasound Transducer Probe Covers?

Natural Rubber Latex Ultrasound Transducer Probe Covers is a medical device that received FDA 510(k) clearance on 2022-06-07. The listed applicant is Global Protection Corp.. The 510(k) number is K213087.

When did Natural Rubber Latex Ultrasound Transducer Probe Covers receive FDA 510(k) clearance?

Natural Rubber Latex Ultrasound Transducer Probe Covers received FDA 510(k) clearance on 2022-06-07, under 510(k) number K213087.

Who is the listed applicant for Natural Rubber Latex Ultrasound Transducer Probe Covers?

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

What is the FDA product code for Natural Rubber Latex Ultrasound Transducer Probe Covers?

The FDA product code for Natural Rubber Latex Ultrasound Transducer Probe Covers is ITX.

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 Global Protection Corp. como candidato(a)

K243972Plain Water-based Lubricant K250142Water-based Lubricant K243967ONE Nitrile Condom K240896ONE Nitrile Condom K223214Powder-Free Nitrile Examination Gloves K203536Male Latex Condom

Ver todos os 8 dispositivos →

Dispositivos Relacionados (Código: ITX)

K260114Align® Cover and Pad Guidance ToolCIVCO Medical Instruments Co., Inc.K261170BA-004CCFujifilm Corporation K254143EM-TECH Passive Ultrasound Probe StrapEM-TECH Solutions, Inc.K260161SmartGuide Disposable Guides and GridsUC-CARE , Ltd.K262474ND Needle Guidance SystemAccurate Access, LLC K261014Accuro® 3S Needle Guide KitRivanna Medical, Inc.

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.