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FDA 510(k)

PLASTIC STOPCOCK W/ EXTENSION TUBE

K-Number: K771911 · 1977-12-08

ApplicantMedon Corp.
Decision Date1977-12-08
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PLASTIC STOPCOCK W/ EXTENSION TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Medon Corp.. It received FDA 510(k) clearance on 1977-12-08 under 510(k) number K771911. 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 PLASTIC STOPCOCK W/ EXTENSION TUBE?

PLASTIC STOPCOCK W/ EXTENSION TUBE is a medical device that received FDA 510(k) clearance on 1977-12-08. The listed applicant is Medon Corp.. The 510(k) number is K771911.

When did PLASTIC STOPCOCK W/ EXTENSION TUBE receive FDA 510(k) clearance?

PLASTIC STOPCOCK W/ EXTENSION TUBE received FDA 510(k) clearance on 1977-12-08, under 510(k) number K771911.

Who is the listed applicant for PLASTIC STOPCOCK W/ EXTENSION TUBE?

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

What is the FDA product code for PLASTIC STOPCOCK W/ EXTENSION TUBE?

The FDA product code for PLASTIC STOPCOCK W/ EXTENSION TUBE is FMG.

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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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