Port Infusion Set (Pis) Infusion Set (Is)

FDA 510(k) K897065 · Prn Services, Inc.

Substantially Equivalent

510(k) numberK897065

Submission

Device name
Port Infusion Set (Pis) Infusion Set (Is)
Applicant
Prn Services, Inc.
Royal Oak, MI, US
Received
December 20, 1989
Decision date
February 16, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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

Other 510(k)s with product code FPA

510(k)DeviceApplicantDecision
K254123Ecomed Disposable Administration SetsFPA · Abbreviated Ecomed Solutions, LLC09/11/2026SE
K261530iiSure Infusion SetFPA · Special Deka Research and Development06/03/2026SE
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
K943206Various TubingFPK · Traditional 03/09/1995SE
K902330E-Z Flo + SetFPA · Traditional 09/21/1990SE
K882598250 ML Bag W/Y Inject. & 12 Extension SetFRN · Traditional 11/01/1988SE
K884053PRN Plus + Infusion SetFPA · Traditional 10/31/1988SE
K87515560 ML Reservoir Bag, Item #200KPE · Traditional 02/16/1988SE
K86022270 ML Reservoir Bag and Administration SetsFRN · Traditional 06/09/1986SE

Questions and answers

When was Port Infusion Set (Pis) Infusion Set (Is) cleared by the FDA?

Port Infusion Set (Pis) Infusion Set (Is) (K897065) received a 510(k) decision of Substantially Equivalent on February 16, 1990, 58 days after the submission was received.

What is the product code of K897065?

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