FDA 510(k)

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

K-Nummer: K161606 · 2017-02-10

Entscheidungsdatum2017-02-10

ProduktcodeFMF

BeratungsausschussHO

EntscheidungSubstantially Equivalent

Produktübersicht

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.

Häufig gestellte Fragen

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.

Zugehörige klinische Studien

Zugehörige Einträge werden automatisch anhand von Namen, Produktcodes oder anderen Metadaten abgeglichen. Eine Übereinstimmung begründet kein verifiziertes klinisches, wissenschaftliches, unternehmerisches oder regulatorisches Verhältnis; prüfen Sie die verlinkten offiziellen Quellen.

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

Weitere Einträge mit Terumo Europe N.V. als Antragsteller

K251447K-Pack Embrace Active Safety Needle (KNAS-2516RB, KNAS-2525RB)K24330927G x 1/2 TW K-Pack Surshield Nadel (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

Alle 7 Geräte anzeigen →

Verwandte Geräte (Code: 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.

Offizielle Quelle

In der FDA-Datenbank anzeigen →

Daten aus der FDA Open API. Für die aktuellsten und verbindlichen Informationen konsultieren Sie bitte stets den offiziellen Datensatz.