FDA 510(k)

QT ECG

Número K: K180157 · 2018-05-04

Data da decisão2018-05-04

Código do produtoDXH

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

QT ECG is the device name listed in this FDA 510(k) record. The listed applicant is QT Medical, Inc.. It received FDA 510(k) clearance on 2018-05-04 under 510(k) number K180157. The device is classified under product code DXH. It was reviewed by the CV advisory panel. Product code DXH falls under the category of Hematology, which includes devices for blood cell counting, coagulation testing, and hemoglobin analysis. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the QT ECG?

QT ECG is a medical device that received FDA 510(k) clearance on 2018-05-04. The listed applicant is QT Medical, Inc.. The 510(k) number is K180157.

When did QT ECG receive FDA 510(k) clearance?

QT ECG received FDA 510(k) clearance on 2018-05-04, under 510(k) number K180157.

Who is the listed applicant for QT ECG?

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

What is the FDA product code for QT ECG?

The FDA product code for QT ECG is DXH. This falls under the Hematology category.

Outros registros que listam QT Medical, Inc. como candidato(a)

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.

K233521QT ECG (QTERD100)K220795QT ECG K200722PCA-C1 series Patient Cable

Dispositivos Relacionados (Código: DXH)

K250233PreemptiveAI Clinical SDKMeasure Labs, Inc. (Dba Preemptiveai, Inc.)K250258HeartBeam AIMIGo with 12-L ECG Synthesis Software SystemHeartbeam, Inc.K243438MEMO Patch M (MPT-E08R-UNC01)Huinno Co., Ltd.K243981Hexoskin Medical System (7100-00016)Carre Technologies, Inc.K243003VitalSigns 1-Lead Holter (VSH101)VitalSigns Technology Co., Ltd.K233521QT ECG (QTERD100)QT 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.