Winged & Subcutaneous Infusion Sets

FDA 510(k) K955709 · Distronic Sterile Products, Inc.

Substantially Equivalent

510(k) numberK955709

Submission

Device name
Winged & Subcutaneous Infusion Sets
Applicant
Distronic Sterile Products, Inc.
Portsmouth, NH, US
Received
December 18, 1995
Decision date
February 21, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FPA – Set, Administration, Intravascular
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5440
Specialty
General Hospital

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K252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072…FPA · Traditional Amsino International, Inc.05/04/2026SE
K251375PuraCath Firefly Needleless Connector IT (9005)FPA · Traditional Puracath Medical, Inc.02/12/2026SE
K251257nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free…FPA · Traditional Np Medical12/04/2025SE
K250325BD Alaris Pump Infusion SetFPA · Traditional Carefusion (Bd)10/30/2025SE
K251814EZ™ IV Administration SetFPA · Traditional Epic Medical Pte. , Ltd.08/29/2025SE
K251854SteadiSet infusion setFPA · Abbreviated Tandem Diabetes Care08/06/2025SE
K243841Sparta Infusion Set for InsulinFPA · Traditional Deka Research and Development08/01/2025SE
K243392Infusomat® Space Volumetric Infusion Pump Administration SetsFPA · Traditional B.Braun Medical, Inc.07/24/2025SE

More from B.Braun Medical, Inc.

510(k)DeviceDecision
K955732Vented Solution SetFPA · Traditional 02/21/1996SE
K954984Minibore Stopcock SetFMG · Traditional 01/23/1996SE
K954983Extension Set with Check ValveFPA · Traditional 01/23/1996SE
K952664Solution Administration SetFPA · Traditional 08/07/1995SE
K950597Core-Resistant Huber Infusion Set with Y-SiteFPA · Traditional 07/26/1995SE
K95266360 Micro Volume Extension Set W/.22 Micron Filter, 21 Extension Set W/1.2 Mivton Gilyrt…FPK · Traditional 07/14/1995SE
K945184Intravascular Administration SetFPK · Traditional 02/08/1995SE

Questions and answers

When was Winged & Subcutaneous Infusion Sets cleared by the FDA?

Winged & Subcutaneous Infusion Sets (K955709) received a 510(k) decision of Substantially Equivalent on February 21, 1996, 65 days after the submission was received.

What is the product code of K955709?

The FDA product code is FPA – Set, Administration, Intravascular, a Class II (moderate risk) device regulated under 21 CFR 880.5440.