FDA 510(k)

MiMo(TM) Negative Pressure Wound Therapy System

Número K: K181929 · 2019-03-27

Data da decisão2019-03-27

Código do produtoOMP

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

MiMo(TM) Negative Pressure Wound Therapy System is the device name listed in this FDA 510(k) record. The listed applicant is Baymax Research, Inc.. It received FDA 510(k) clearance on 2019-03-27 under 510(k) number K181929. The device is classified under product code OMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the MiMo(TM) Negative Pressure Wound Therapy System?

MiMo(TM) Negative Pressure Wound Therapy System is a medical device that received FDA 510(k) clearance on 2019-03-27. The listed applicant is Baymax Research, Inc.. The 510(k) number is K181929.

When did MiMo(TM) Negative Pressure Wound Therapy System receive FDA 510(k) clearance?

MiMo(TM) Negative Pressure Wound Therapy System received FDA 510(k) clearance on 2019-03-27, under 510(k) number K181929.

Who is the listed applicant for MiMo(TM) Negative Pressure Wound Therapy System?

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

What is the FDA product code for MiMo(TM) Negative Pressure Wound Therapy System?

The FDA product code for MiMo(TM) Negative Pressure Wound Therapy System is OMP.

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: OMP)

K261338RENASYS DYNAFLOW Kit (66807741)Smith & Nephew Medical, Ltd.K253263ConvaVAC™ Negative Pressure Wound Therapy SystemConvatec Limited, Gdc Building K253199CURASYS 2 (EMDN0003)CG Bio Co., Ltd.K260646RENASYS EDGE (66803126)Smith & Nephew Medical, Ltd.K261291Nisus NPWT Canister 500-mL (CPC-500)Cork Medical K254019Wound Geni NPWT SystemBechtel 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.