FDA 510(k)

V-PVP

Número K: K232125 · 2024-03-20

Data da decisão2024-03-20

Código do produtoMQL

Comité consultivoOB

DecisãoSubstantially Equivalent

Resumo do dispositivo

V-PVP is the device name listed in this FDA 510(k) record. The listed applicant is Vitromed GmbH. It received FDA 510(k) clearance on 2024-03-20 under 510(k) number K232125. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the V-PVP?

V-PVP is a medical device that received FDA 510(k) clearance on 2024-03-20. The listed applicant is Vitromed GmbH. The 510(k) number is K232125.

When did V-PVP receive FDA 510(k) clearance?

V-PVP received FDA 510(k) clearance on 2024-03-20, under 510(k) number K232125.

Who is the listed applicant for V-PVP?

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

What is the FDA product code for V-PVP?

The FDA product code for V-PVP is MQL.

Outros registros que listam Vitromed GmbH 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.

K241833V-GRAD K240176V-VITFREEZE and V-VITWARM K222606V-HYADASE K223117V-SPERM WASH K193285V-ONESTEP K192146V-DENUPET

Ver todos os 7 dispositivos →

Dispositivos Relacionados (Código: MQL)

K254261Vitrification Freeze Kit and Thawing Kit (CS-IVF-FK; CS-IVF-TK)CELL STORE (BEIJING) BIOTECHNOLOGY CO., LTD.K260248Ultra-Fast WarmKitazato Corporation K252672CaseBio™ Culture w/HSA (CMH5); CaseBio™ Handling w/HSA (WHH5)Casebioscience, Inc.K250445Fast Warm - NXFujifilm Irvine Scientific K251637Dewin Reproductive Media (Dewin Gamete Buffer [with HSA and without HSA]; Dewin Follicle Flushing Solution, Dewin One Step medium [with HSA and without HSA])Donnevie Medical Technology (Shanghai) Co. , Ltd.K251305Ultra-Fast Vitri; Ultra-Fast WarmKitazato Corporation

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.