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FDA 510(k)

STOPCOCKS & EXTENSION TUBES

K-Number: K840394 · 1984-03-19

ApplicantAmerican Pharmaseal Div. Ahsc
Decision Date1984-03-19
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STOPCOCKS & EXTENSION TUBES is the device name listed in this FDA 510(k) record. The listed applicant is American Pharmaseal Div. Ahsc. It received FDA 510(k) clearance on 1984-03-19 under 510(k) number K840394. 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 STOPCOCKS & EXTENSION TUBES?

STOPCOCKS & EXTENSION TUBES is a medical device that received FDA 510(k) clearance on 1984-03-19. The listed applicant is American Pharmaseal Div. Ahsc. The 510(k) number is K840394.

When did STOPCOCKS & EXTENSION TUBES receive FDA 510(k) clearance?

STOPCOCKS & EXTENSION TUBES received FDA 510(k) clearance on 1984-03-19, under 510(k) number K840394.

Who is the listed applicant for STOPCOCKS & EXTENSION TUBES?

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

What is the FDA product code for STOPCOCKS & EXTENSION TUBES?

The FDA product code for STOPCOCKS & EXTENSION TUBES 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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