FDA 510(k)

Clicky Cross

K-Nummer: K210516 · 2022-05-16

Entscheidungsdatum2022-05-16

ProduktcodeFMG

BeratungsausschussHO

EntscheidungSubstantially Equivalent

Produktübersicht

Clicky Cross is the device name listed in this FDA 510(k) record. The listed applicant is Yomura Technologies, Inc.. It received FDA 510(k) clearance on 2022-05-16 under 510(k) number K210516. The device is classified under product code FMG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Häufig gestellte Fragen

What is the Clicky Cross?

Clicky Cross is a medical device that received FDA 510(k) clearance on 2022-05-16. The listed applicant is Yomura Technologies, Inc.. The 510(k) number is K210516.

When did Clicky Cross receive FDA 510(k) clearance?

Clicky Cross received FDA 510(k) clearance on 2022-05-16, under 510(k) number K210516.

Who is the listed applicant for Clicky Cross?

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

What is the FDA product code for Clicky Cross?

The FDA product code for Clicky Cross is FMG.

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

Verwandte Geräte (Code: FMG)

K242255Qitexio® 4-Way Stopcock (QIT014)Medex K223499Three Way Stop CockM/S Romsons International K223175lntravascular Administration Sets with Stopcock and ManifoldBaxter Healthcare Corporation K211204SafePort(TM) Manifold (or Stopcock)Elcam Medical Acal K190539TurnSignal Stopcocks Sterile, TurnSignal Stopcocks Buld Non Sterile, TurnSignal Stopcocks with Manifolds Sterile, TurnSignal Stopcocks with Manifolds Bulk Non SterileMonumedical, LLC K190489Elcam Stopcocks and ManifoldsElcam Medical Acal

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.