FDA 510(k)

Zyppah Anti-Snoring Device

Número K: K182312 · 2019-01-24

Data da decisão2019-01-24

Código do produtoLRK

Comité consultivoDE

DecisãoSubstantially Equivalent

Resumo do dispositivo

Zyppah Anti-Snoring Device is the device name listed in this FDA 510(k) record. The listed applicant is Always More Marketing. It received FDA 510(k) clearance on 2019-01-24 under 510(k) number K182312. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Zyppah Anti-Snoring Device?

Zyppah Anti-Snoring Device is a medical device that received FDA 510(k) clearance on 2019-01-24. The listed applicant is Always More Marketing. The 510(k) number is K182312.

When did Zyppah Anti-Snoring Device receive FDA 510(k) clearance?

Zyppah Anti-Snoring Device received FDA 510(k) clearance on 2019-01-24, under 510(k) number K182312.

Who is the listed applicant for Zyppah Anti-Snoring Device?

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

What is the FDA product code for Zyppah Anti-Snoring Device?

The FDA product code for Zyppah Anti-Snoring Device is LRK.

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: LRK)

K262104Anti Snoring Mouthpiece (L09-BB, L09-PP, L09-TB, L09-BT, L09-TP, L09-PT, L09-TT)Ram.Shaw Pte., Ltd.K261912SnØreNegatØrDnB Innovations, LLC K261366VirtusSomnomed, Inc.K261251Snorbliss® Anti-Snoring DeviceEndeavor Commerce, LLC K261134Dormiva Anti-Snoring Mouth GuardKoncept Innovators, Inc.K252942ShaeferHShaeferh, LLC

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.