FDA 510(k)

DABRA Laser System (DABRA Laser model RA-308 and DABRA Catheter model 101)

Número K: K210664 · 2021-07-27

Data da decisão2021-07-27

Código do produtoPDU

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

DABRA Laser System (DABRA Laser model RA-308 and DABRA Catheter model 101) is the device name listed in this FDA 510(k) record. The listed applicant is Ra Medical Systems,Inc. It received FDA 510(k) clearance on 2021-07-27 under 510(k) number K210664. The device is classified under product code PDU. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the DABRA Laser System (DABRA Laser model RA-308 and DABRA Catheter model 101)?

DABRA Laser System (DABRA Laser model RA-308 and DABRA Catheter model 101) is a medical device that received FDA 510(k) clearance on 2021-07-27. The listed applicant is Ra Medical Systems,Inc. The 510(k) number is K210664.

When did DABRA Laser System (DABRA Laser model RA-308 and DABRA Catheter model 101) receive FDA 510(k) clearance?

DABRA Laser System (DABRA Laser model RA-308 and DABRA Catheter model 101) received FDA 510(k) clearance on 2021-07-27, under 510(k) number K210664.

Who is the listed applicant for DABRA Laser System (DABRA Laser model RA-308 and DABRA Catheter model 101)?

The FDA 510(k) record lists Ra Medical Systems,Inc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DABRA Laser System (DABRA Laser model RA-308 and DABRA Catheter model 101)?

The FDA product code for DABRA Laser System (DABRA Laser model RA-308 and DABRA Catheter model 101) is PDU.

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 Ra Medical Systems,Inc como candidato(a)

K220544DABRA Excimer Laser System (DABRA Laser model RA-308 and DABRA Catheter model 2.0)K170349RA-308 Excimer Laser System, Excimer Laser Catheter

Dispositivos Relacionados (Código: PDU)

K262013Kiba CTO Crossing CatheterReflow Medical, Inc.K252315Santreva™-ATK Endovascular Revasculariztion CatheterAngioSafe, Inc.K251158PowerWire® 14 Radiofrequency Guidewire KitBaylis Medical Technologies, Inc.K251376LimFlow ARCLimFlow, Inc.K232562PowerWire Radiofrequency Guidewire KitBaylis Medical Technologies, Inc.K230159SoundBite® Crossing System XS PeripheralSoundbite Medical Solutions, 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.