FDA 510(k)

Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit

Número K: K232443 · 2023-09-07

Data da decisão2023-09-07

Código do produtoMMX

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit is the device name listed in this FDA 510(k) record. The listed applicant is Argon Medical Devices, Inc.. It received FDA 510(k) clearance on 2023-09-07 under 510(k) number K232443. The device is classified under product code MMX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit?

Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit is a medical device that received FDA 510(k) clearance on 2023-09-07. The listed applicant is Argon Medical Devices, Inc.. The 510(k) number is K232443.

When did Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit receive FDA 510(k) clearance?

Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit received FDA 510(k) clearance on 2023-09-07, under 510(k) number K232443.

Who is the listed applicant for Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit?

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

What is the FDA product code for Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit?

The FDA product code for Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit is MMX.

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

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

K252795ZeniCore™ Automatic Biopsy Instrument (863212100 / ZeniCore Automatic Biopsy Device 12ga x 10cm with Coaxial Introducer Kit); ZeniCore™ Automatic Biopsy Instrument (863212130 / ZeniCore Automatic Biopsy Device 12ga x 13cm with Coaxial Introducer Kit); ZeniCore™ Automatic Biopsy Instrument (863214100 / ZeniCore Automatic Biopsy Device 14ga x 10cm with Coaxial Introducer Kit); ZeniCore™ Automatic Biopsy Instrument (863214130 / ZeniCore Automatic Biopsy Device 14ga x 13cm with Coaxial K260028CLEANER™ Vac Thrombectomy System, CLEANER™ Vac Aspiration Catheter with Handpiece, CLEANER™ Vac Aspiration Canister K251318VariFuse Adjustable Infusion Catheter K253741V•Stick™ Vascular Access Set K242612Option ELITE Vena Cava Filter System (352506070E 352506100E)K241145TLAB® Transvenous Liver Biopsy System (TF-18C)

Ver todos os 18 dispositivos →

Dispositivos Relacionados (Código: MMX)

K242776LimFlow V-CeiverLimFlow, Inc.K241259Kit de Sinais de Ganso AmplatzMedtronic, Inc.K222254Gunther Tulip Vena Cava Filter Retrieval SetCook Incorporated K222083LimFlow V-CeiverLimFlow, Inc.K212988ONO Retrieval DeviceOnocor Vascular, LLC K213494Aveir Retrieval CatheterABBOTT MEDICAL

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.