FDA 510(k)

Conjunto de Cateter de Bloqueio Nervoso Ancora

Número K: K191290 · 2020-02-06

Data da decisão2020-02-06

Código do produtoBSP

Comité consultivoAN

DecisãoSubstantially Equivalent

Resumo do dispositivo

Ancora Nerve Block Catheter Set is the device name listed in this FDA 510(k) record. The listed applicant is Ancora Medical Technology. It received FDA 510(k) clearance on 2020-02-06 under 510(k) number K191290. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Ancora Nerve Block Catheter Set?

Ancora Nerve Block Catheter Set is a medical device that received FDA 510(k) clearance on 2020-02-06. The listed applicant is Ancora Medical Technology. The 510(k) number is K191290.

When did Ancora Nerve Block Catheter Set receive FDA 510(k) clearance?

Ancora Nerve Block Catheter Set received FDA 510(k) clearance on 2020-02-06, under 510(k) number K191290.

Who is the listed applicant for Ancora Nerve Block Catheter Set?

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

What is the FDA product code for Ancora Nerve Block Catheter Set?

The FDA product code for Ancora Nerve Block Catheter Set is BSP.

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: BSP)

K243690SonoMSKPAJUNK GmbH Medizintechnologie K243682SonoPlex STIM; SonoPlex IIPAJUNK GmbH Medizintechnologie K250774SPROTTE® STANDARD (LUER/ NRFit®) Lumbar PuncturePAJUNK GmbH Medizintechnologie K243525SonoTAP and SonoTAP IIPAJUNK GmbH Medizintechnologie K241953SPROTTE® STANDARD (LUER/ NRFit®) AnesthesiologyPAJUNK GmbH Medizintechnologie K241954SonoBlock; SonoBlock IIPAJUNK GmbH Medizintechnologie

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.