FDA 510(k)

STOPCOCKS

K-Number: K851986 · 1985-05-23

Decision Date1985-05-23

Product CodeFMG

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

STOPCOCKS is the device name listed in this FDA 510(k) record. The listed applicant is Transamerica Delaval, Inc.. It received FDA 510(k) clearance on 1985-05-23 under 510(k) number K851986. 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?

STOPCOCKS is a medical device that received FDA 510(k) clearance on 1985-05-23. The listed applicant is Transamerica Delaval, Inc.. The 510(k) number is K851986.

When did STOPCOCKS receive FDA 510(k) clearance?

STOPCOCKS received FDA 510(k) clearance on 1985-05-23, under 510(k) number K851986.

Who is the listed applicant for STOPCOCKS?

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

What is the FDA product code for STOPCOCKS?

The FDA product code for STOPCOCKS is FMG.

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Other records listing Transamerica Delaval, Inc. as applicant

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Related Devices (Code: FMG)

K242255Qitexio® 4-Way Stopcock (QIT014)Medex K223499Three Way Stop CockM/S Romsons International K223175lntravascular Administration Sets with Stopcock and ManifoldBaxter Healthcare Corporation K211204SafePort(TM) Manifold (or Stopcock)Elcam Medical Acal K210516Clicky 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.