TurnSignal Stopcocks Sterile, TurnSignal Stopcocks Buld Non Sterile, TurnSignal Stopcocks with Manifolds Sterile, TurnSignal Stopcocks with Manifolds Bulk Non Sterile

FDA 510(k) K190539 · Monumedical, LLC

Substantially Equivalent

510(k) numberK190539

Submission

Device name
TurnSignal Stopcocks Sterile, TurnSignal Stopcocks Buld Non Sterile, TurnSignal Stopcocks with Manifolds Sterile, TurnSignal Stopcocks with Manifolds Bulk Non Sterile
Applicant
Monumedical, LLC
Roseville, CA, US
Received
March 4, 2019
Decision date
October 22, 2019
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FMG – Stopcock, I.V. Set
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5440
Specialty
General Hospital

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K223175lntravascular Administration Sets with Stopcock and ManifoldFMG · Traditional Baxter Healthcare Corporation03/10/2023SE
K211204SafePort(TM) Manifold (or Stopcock)FMG · Traditional Elcam Medical Acal09/15/2022SE
K210516Clicky CrossFMG · Traditional Yomura Technologies, Inc.05/16/2022SE
K190489Elcam Stopcocks and ManifoldsFMG · Special Elcam Medical Acal04/23/2019SE
K172266Dynarex Three-Way StopcockFMG · Traditional Dynarex Corporation03/14/2018SE
K141254Elcam Stopcocks and ManifoldsFMG · Special Elcam Medical Acal07/30/2014SE
K123084Disposable High Pressure Stopcock/Manifold Model HP Stopcock, MP Stopcock, HP Manifold…FMG · Traditional Elcam Medical Acal05/23/2013SE
K130245Large Bore Stopcock with Rotating Male Luer Lock/Large Bore Stopcock with Extension Set…FMG · Special Baxter Healthcare Corp03/01/2013SE

Questions and answers

When was TurnSignal Stopcocks Sterile, TurnSignal Stopcocks Buld Non Sterile, TurnSignal Stopcocks with Manifolds Sterile, TurnSignal Stopcocks with Manifolds Bulk Non Sterile cleared by the FDA?

TurnSignal Stopcocks Sterile, TurnSignal Stopcocks Buld Non Sterile, TurnSignal Stopcocks with Manifolds Sterile, TurnSignal Stopcocks with Manifolds Bulk Non Sterile (K190539) received a 510(k) decision of Substantially Equivalent on October 22, 2019, 232 days after the submission was received.

What is the product code of K190539?

The FDA product code is FMG – Stopcock, I.V. Set, a Class II (moderate risk) device regulated under 21 CFR 880.5440.