Bacstop

FDA 510(k) K053405 · Elcam Medical Acal

Substantially Equivalent

510(k) numberK053405

Submission

Device name
Bacstop
Applicant
Elcam Medical Acal
Mp. Merom Hagalil, IL
Received
December 7, 2005
Decision date
May 11, 2006
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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K141254Elcam Stopcocks and ManifoldsFMG · Special 07/30/2014SE
K123084Disposable High Pressure Stopcock/Manifold Model HP Stopcock, MP Stopcock, HP Manifold…FMG · Traditional 05/23/2013SE
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K111467Flexi-Q DV and DVR Auto-InjectorsKZH · Traditional 02/09/2012SE
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Questions and answers

When was Bacstop cleared by the FDA?

Bacstop (K053405) received a 510(k) decision of Substantially Equivalent on May 11, 2006, 155 days after the submission was received.

What is the product code of K053405?

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