Large Bore Stopcock with Rotating Male Luer Lock/Large Bore Stopcock with Extension Set, Gang Large Bore Stopcock Manifo

FDA 510(k) K130245 · Baxter Healthcare Corp

Substantially Equivalent

510(k) numberK130245

Submission

Device name
Large Bore Stopcock with Rotating Male Luer Lock/Large Bore Stopcock with Extension Set, Gang Large Bore Stopcock Manifo
Applicant
Baxter Healthcare Corp
Round Lake, IL, US
Received
January 31, 2013
Decision date
March 1, 2013
Decision
Substantially Equivalent (SESE)
Type
Special 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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Questions and answers

When was Large Bore Stopcock with Rotating Male Luer Lock/Large Bore Stopcock with Extension Set, Gang Large Bore Stopcock Manifo cleared by the FDA?

Large Bore Stopcock with Rotating Male Luer Lock/Large Bore Stopcock with Extension Set, Gang Large Bore Stopcock Manifo (K130245) received a 510(k) decision of Substantially Equivalent on March 1, 2013, 29 days after the submission was received.

What is the product code of K130245?

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