Three Way Stop Cock

FDA 510(k) K223499 · M/S Romsons International

Substantially Equivalent

510(k) numberK223499

Submission

Device name
Three Way Stop Cock
Applicant
M/S Romsons International
Noida, IN
Received
November 21, 2022
Decision date
July 21, 2023
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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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
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Questions and answers

When was Three Way Stop Cock cleared by the FDA?

Three Way Stop Cock (K223499) received a 510(k) decision of Substantially Equivalent on July 21, 2023, 242 days after the submission was received.

What is the product code of K223499?

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