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FDA 510(k)

4-WAY STOPCOCK W/100 CM TUBING, LUER-LK

K-Number: K760678 · 1976-12-02

ApplicantAmerican Viggo
Decision Date1976-12-02
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

4-WAY STOPCOCK W/100 CM TUBING, LUER-LK is the device name listed in this FDA 510(k) record. The listed applicant is American Viggo. It received FDA 510(k) clearance on 1976-12-02 under 510(k) number K760678. 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 4-WAY STOPCOCK W/100 CM TUBING, LUER-LK?

4-WAY STOPCOCK W/100 CM TUBING, LUER-LK is a medical device that received FDA 510(k) clearance on 1976-12-02. The listed applicant is American Viggo. The 510(k) number is K760678.

When did 4-WAY STOPCOCK W/100 CM TUBING, LUER-LK receive FDA 510(k) clearance?

4-WAY STOPCOCK W/100 CM TUBING, LUER-LK received FDA 510(k) clearance on 1976-12-02, under 510(k) number K760678.

Who is the listed applicant for 4-WAY STOPCOCK W/100 CM TUBING, LUER-LK?

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

What is the FDA product code for 4-WAY STOPCOCK W/100 CM TUBING, LUER-LK?

The FDA product code for 4-WAY STOPCOCK W/100 CM TUBING, LUER-LK is FMG.

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Other records listing American Viggo 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.

K771339MALE LUER LOCK PLUGK770528NEEDLE, MEMBRANEK770174LUER-LOCK EXTENSION SETK770181I.V. CATHETER PLACEMENT UNITK7701543-WAY STOPCOCK WITH LUER-LOCK FITTINGK770096EPIDURAL BLOCK PROCEDURE PACK

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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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