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FDA 510(k)

TU STOPCOCK

K-Number: K881805 · 1988-10-04

ApplicantTulan Corp. C/O Richard Hamer Assoc.
Decision Date1988-10-04
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TU STOPCOCK is the device name listed in this FDA 510(k) record. The listed applicant is Tulan Corp. C/O Richard Hamer Assoc.. It received FDA 510(k) clearance on 1988-10-04 under 510(k) number K881805. 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 TU STOPCOCK?

TU STOPCOCK is a medical device that received FDA 510(k) clearance on 1988-10-04. The listed applicant is Tulan Corp. C/O Richard Hamer Assoc.. The 510(k) number is K881805.

When did TU STOPCOCK receive FDA 510(k) clearance?

TU STOPCOCK received FDA 510(k) clearance on 1988-10-04, under 510(k) number K881805.

Who is the listed applicant for TU STOPCOCK?

The FDA 510(k) record lists Tulan Corp. C/O Richard Hamer Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TU STOPCOCK?

The FDA product code for TU STOPCOCK is FMG.

Related Clinical Trials

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.

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Other records listing Tulan Corp. C/O Richard Hamer Assoc. 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.

K884944TU SUCTIONTRAP

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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