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FDA 510(k)

TRI-FLOW THREE WAY STOPCOCK

K-Number: K961982 · 1997-02-21

ApplicantNorth, Inc.
Decision Date1997-02-21
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TRI-FLOW THREE WAY STOPCOCK is the device name listed in this FDA 510(k) record. The listed applicant is North, Inc.. It received FDA 510(k) clearance on 1997-02-21 under 510(k) number K961982. The device is classified under product code FMG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRI-FLOW THREE WAY STOPCOCK?

TRI-FLOW THREE WAY STOPCOCK is a medical device that received FDA 510(k) clearance on 1997-02-21. The listed applicant is North, Inc.. The 510(k) number is K961982.

When did TRI-FLOW THREE WAY STOPCOCK receive FDA 510(k) clearance?

TRI-FLOW THREE WAY STOPCOCK received FDA 510(k) clearance on 1997-02-21, under 510(k) number K961982.

Who is the listed applicant for TRI-FLOW THREE WAY STOPCOCK?

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

What is the FDA product code for TRI-FLOW THREE WAY STOPCOCK?

The FDA product code for TRI-FLOW THREE WAY STOPCOCK is FMG.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing North, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K954189EASI-JECTOR CONTROL SYSTEM

Related Devices (Code: FMG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K242255Qitexio® 4-Way Stopcock (QIT014)MedexK223499Three Way Stop CockM/S Romsons InternationalK223175lntravascular Administration Sets with Stopcock and ManifoldBaxter Healthcare CorporationK211204SafePort(TM) Manifold (or Stopcock)Elcam Medical AcalK210516Clicky CrossYomura Technologies, Inc.K190539TurnSignal Stopcocks Sterile, TurnSignal Stopcocks Buld Non Sterile, TurnSignal Stopcocks with Manifolds Sterile, TurnSignal Stopcocks with Manifolds Bulk Non SterileMonumedical, LLC

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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