FDA 510(k)

UltraThineer Zirconia Slurry (5Y-B)

Número K: K240419 · 2024-04-12

Data da decisão2024-04-12

Código do produtoEIH

Comité consultivoDE

DecisãoSubstantially Equivalent

Resumo do dispositivo

UltraThineer Zirconia Slurry (5Y-B) is the device name listed in this FDA 510(k) record. The listed applicant is Boston Micro Fabrication. It received FDA 510(k) clearance on 2024-04-12 under 510(k) number K240419. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the UltraThineer Zirconia Slurry (5Y-B)?

UltraThineer Zirconia Slurry (5Y-B) is a medical device that received FDA 510(k) clearance on 2024-04-12. The listed applicant is Boston Micro Fabrication. The 510(k) number is K240419.

When did UltraThineer Zirconia Slurry (5Y-B) receive FDA 510(k) clearance?

UltraThineer Zirconia Slurry (5Y-B) received FDA 510(k) clearance on 2024-04-12, under 510(k) number K240419.

Who is the listed applicant for UltraThineer Zirconia Slurry (5Y-B)?

The FDA 510(k) record lists Boston Micro Fabrication as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UltraThineer Zirconia Slurry (5Y-B)?

The FDA product code for UltraThineer Zirconia Slurry (5Y-B) is EIH.

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: EIH)

K262074Any-ZircosMediclus Co., Ltd.K262239Obsidian® Press Over ZirconiaPrismatik Dentalcraft, Inc.K261046Dental Zirconia Blank & Coloring LiquidHunan Qinghao Puzhong Technology Co., Ltd.K262195Dandy Ceramic Stain and GlazeZima International Inc., dba Dandy K260918Zolid LunarisAmann Girrbach AG K260859Rosetta SM, Rosetta SPHass Corp.

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.