FDA 510(k)

Syringe with fixed needle - For use only with GONAL-F Multi-Dose 600 I/U mL FSH

Número K: K161606 · 2017-02-10

Data da decisão2017-02-10

Código do produtoFMF

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Syringe with fixed needle - For use only with GONAL-F Multi-Dose 600 I/U mL FSH is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Europe N.V.. It received FDA 510(k) clearance on 2017-02-10 under 510(k) number K161606. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Syringe with fixed needle - For use only with GONAL-F Multi-Dose 600 I/U mL FSH?

Syringe with fixed needle - For use only with GONAL-F Multi-Dose 600 I/U mL FSH is a medical device that received FDA 510(k) clearance on 2017-02-10. The listed applicant is Terumo Europe N.V.. The 510(k) number is K161606.

When did Syringe with fixed needle - For use only with GONAL-F Multi-Dose 600 I/U mL FSH receive FDA 510(k) clearance?

Syringe with fixed needle - For use only with GONAL-F Multi-Dose 600 I/U mL FSH received FDA 510(k) clearance on 2017-02-10, under 510(k) number K161606.

Who is the listed applicant for Syringe with fixed needle - For use only with GONAL-F Multi-Dose 600 I/U mL FSH?

The FDA 510(k) record lists Terumo Europe N.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Syringe with fixed needle - For use only with GONAL-F Multi-Dose 600 I/U mL FSH?

The FDA product code for Syringe with fixed needle - For use only with GONAL-F Multi-Dose 600 I/U mL FSH is FMF.

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 Terumo Europe N.V. como candidato(a)

K251447K-Pack Embrace Active Safety Needle (KNAS-2516RB, KNAS-2525RB)K24330927G x 1/2 TW K-Pack Surshield Needle (KN-S2713RBT)K243581K-Pack Enhance Needle (KH-2713RBBTC and KH-2913RBBTC)K230951Terumo Injection Filter Needle (NF-3013RBKE05M)K212095SurGuard3 Safety Hypodermic Needle K192057K-Pack II Needle - 27G x 1/2” Extra Thin Wall, K-Pack II Needle - 27G x 1/2” Ultra Thin Wall, K-Pack II Needle - 30G x 1/2” Extra Thin Wall, K-Pack II Needle - 30G x 1/2” Ultra Thin Wall

Ver todos os 7 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.

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.