FDA 510(k)

GPS Advanced; 5 cc GPS Advanced Cannula

N.º K: K241426 · 2024-07-10

Fecha de decisión2024-07-10

Código de productoFMF

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

GPS Advanced; 5 cc GPS Advanced Cannula is the device name listed in this FDA 510(k) record. The listed applicant is Prosidyan, Inc.. It received FDA 510(k) clearance on 2024-07-10 under 510(k) number K241426. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the GPS Advanced; 5 cc GPS Advanced Cannula?

GPS Advanced; 5 cc GPS Advanced Cannula is a medical device that received FDA 510(k) clearance on 2024-07-10. The listed applicant is Prosidyan, Inc.. The 510(k) number is K241426.

When did GPS Advanced; 5 cc GPS Advanced Cannula receive FDA 510(k) clearance?

GPS Advanced; 5 cc GPS Advanced Cannula received FDA 510(k) clearance on 2024-07-10, under 510(k) number K241426.

Who is the listed applicant for GPS Advanced; 5 cc GPS Advanced Cannula?

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

What is the FDA product code for GPS Advanced; 5 cc GPS Advanced Cannula?

The FDA product code for GPS Advanced; 5 cc GPS Advanced Cannula is FMF.

Ensayos clínicos relacionados

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

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

Otros registros que enlistan a Prosidyan, Inc. como solicitante

K253147FIBERGRAFT™ BG Putty GPS Bone Graft Substitute FIBERGRAFT™ BG Putty Bone Graft Substitute FIBERGRAFT™ AERIDYAN™ Matrix Bone Graft Substitute FIBERGRAFT™ BG Matrix Bone Graft Substitute K251648GPS Advanced; GPS Advanced Cannula K213803FIBERGRAFT Aeridyan Matrix Bone Graft Substitute K182670FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute K180080FIBERGRAFT BG Matrix Bone Graft Substitute K171284FIBERGRAFT BG Matrix Bone Graft Substitute

Ver todos los 8 dispositivos →

Dispositivos relacionados (Código: FMF)

K262581GraftGun Universal Graft Delivery System (GDS®)SurGenTec, LLC K252184SOL-M Luer Lock Syringe with Exchangeable Needle TraySol-Millennium Medical, Inc.K253747Disposable Pen Injector (KXYC-03C02, KXYC-03A03)Jiangsu Enjosim Medical Technology Co., Ltd.K260208Ultra-Fine™ SAFETY Insulin Syringeembecta Medical II, LLC K253110Sol-Glide Safety Needle; Sol-Glide Safety Needle with SyringeSol-Millennium Medical, Inc.K260514Profoject™ Safety Needle; Profoject™ Syringe with Safety Needle; Profoject™ Low Dead Space Syringe with Safety NeedleCMT Health PTE., Ltd.

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.