FDA 510(k)

The Red Head Collection Device, The Jordy Connection System

Número K: K161372 · 2017-02-24

Data da decisão2017-02-24

Código do produtoMUU

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

The Red Head Collection Device, The Jordy Connection System is the device name listed in this FDA 510(k) record. The listed applicant is Miami Fat Supply. It received FDA 510(k) clearance on 2017-02-24 under 510(k) number K161372. The device is classified under product code MUU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the The Red Head Collection Device, The Jordy Connection System?

The Red Head Collection Device, The Jordy Connection System is a medical device that received FDA 510(k) clearance on 2017-02-24. The listed applicant is Miami Fat Supply. The 510(k) number is K161372.

When did The Red Head Collection Device, The Jordy Connection System receive FDA 510(k) clearance?

The Red Head Collection Device, The Jordy Connection System received FDA 510(k) clearance on 2017-02-24, under 510(k) number K161372.

Who is the listed applicant for The Red Head Collection Device, The Jordy Connection System?

The FDA 510(k) record lists Miami Fat Supply as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for The Red Head Collection Device, The Jordy Connection System?

The FDA product code for The Red Head Collection Device, The Jordy Connection System is MUU.

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: MUU)

K210528IntelliFat Disposable Adipose Tissue Harvesting and Transfer Kit, IntelliFat Body On Demand (BOD) KitMillennium Medical Technologies Inc (Dba Cellmyx)K203800SyntrFuge SystemSyntr Health Technologies, Inc.K202443Smart Kit Basic, Smart Kit ProBsl Co., Ltd.K193539REVOLVE ENVI 600 Advanced Adipose SystemLifecell Corporation K193363Dermapose RefreshPuregraft, LLC K182732JTL-250-01Jointechlabs, 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.