FDA 510(k)

NAR Sharps Shuttle; NAR Sharps Shuttle Pack of six

Número K: K152340 · 2016-05-31

Data da decisão2016-05-31

Código do produtoMMK

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

NAR Sharps Shuttle; NAR Sharps Shuttle Pack of six is the device name listed in this FDA 510(k) record. The listed applicant is North American Rescue, LLC. It received FDA 510(k) clearance on 2016-05-31 under 510(k) number K152340. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the NAR Sharps Shuttle; NAR Sharps Shuttle Pack of six?

NAR Sharps Shuttle; NAR Sharps Shuttle Pack of six is a medical device that received FDA 510(k) clearance on 2016-05-31. The listed applicant is North American Rescue, LLC. The 510(k) number is K152340.

When did NAR Sharps Shuttle; NAR Sharps Shuttle Pack of six receive FDA 510(k) clearance?

NAR Sharps Shuttle; NAR Sharps Shuttle Pack of six received FDA 510(k) clearance on 2016-05-31, under 510(k) number K152340.

Who is the listed applicant for NAR Sharps Shuttle; NAR Sharps Shuttle Pack of six?

The FDA 510(k) record lists North American Rescue, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NAR Sharps Shuttle; NAR Sharps Shuttle Pack of six?

The FDA product code for NAR Sharps Shuttle; NAR Sharps Shuttle Pack of six is MMK.

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: MMK)

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.