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FDA 510(k)

TERUFUSION THREE WAY STOPCOCK

K-Number: K891234 · 1989-09-19

ApplicantTerumo Medical Corp.
Decision Date1989-09-19
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TERUFUSION THREE WAY STOPCOCK is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Medical Corp.. It received FDA 510(k) clearance on 1989-09-19 under 510(k) number K891234. 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 TERUFUSION THREE WAY STOPCOCK?

TERUFUSION THREE WAY STOPCOCK is a medical device that received FDA 510(k) clearance on 1989-09-19. The listed applicant is Terumo Medical Corp.. The 510(k) number is K891234.

When did TERUFUSION THREE WAY STOPCOCK receive FDA 510(k) clearance?

TERUFUSION THREE WAY STOPCOCK received FDA 510(k) clearance on 1989-09-19, under 510(k) number K891234.

Who is the listed applicant for TERUFUSION THREE WAY STOPCOCK?

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

What is the FDA product code for TERUFUSION THREE WAY STOPCOCK?

The FDA product code for TERUFUSION THREE WAY STOPCOCK is FMG.

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Other records listing Terumo Medical Corp. 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.

K111606PINNACLE PRECISION ACCESS SYSTEMK111556GLIDECROSS SUPPORT CATHETERK110540TERUMO SUPPORT CATHETERK102008GLIDESHEATHK091329PINNACLE DESTINATION PERIPHERAL GUIDING SHEATHK082997TERUMO HYBRIA CLOSED SYSTEM SAFETY I.V. CATHETER

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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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