Assyro AI
510(k) Predicate Database
FDA 510(k) ClearanceFPA

ProSeal™ Closed System Administration Set

FDA 510(k) K230343 · Epic Medical Pte. , Ltd.

510(k) number
K230343
Device name
ProSeal™ Closed System Administration Set
Applicant
Epic Medical Pte. , Ltd.
Product code
FPA
Decision
Substantially Equivalent
Decision date
2023-11-03
Device class
Class 2
Regulation number
880.5440
Advisory committee
General Hospital
Medical specialty
General Hospital

Candidate predicate devices

Other devices cleared under product code FPA — the same regulatory device type, and therefore candidate predicates for a substantial-equivalence comparison. Confirm each predicate is legally marketed before relying on it.

510(k)DeviceApplicantDecision date
K261530iiSure Infusion SetDeka Research and Development2026-06-03
K252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)Amsino International, Inc.2026-05-04
K251375PuraCath Firefly Needleless Connector IT (9005)Puracath Medical, Inc.2026-02-12
K251257nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free Connector (NFC) [6426731]; nSyte Needle Free Connector (NFC) [6426727]Np Medical2025-12-04
K250325BD Alaris Pump Infusion SetCarefusion (Bd)2025-10-30
K251814EZ™ IV Administration SetEpic Medical Pte. , Ltd.2025-08-29
K251854SteadiSet infusion setTandem Diabetes Care2025-08-06
K243841Sparta Infusion Set for InsulinDeka Research and Development2025-08-01
K243392Infusomat® Space Volumetric Infusion Pump Administration SetsB.Braun Medical, Inc.2025-07-24
K250616Clave™ Neutral-Displacement Needlefree ConnectorsIcu Medical, Inc.2025-06-05
K242692SteadiSet Infusion SetCapillary Biomedical, LLC2025-05-09
K242763JetCan® Pro Safety Huber NeedlePfm Medical, Inc.2025-05-02

Building a 510(k) around this device type?

Assyro turns predicate research into a substantial-equivalence comparison and an eSTAR-ready 510(k) workflow — so predicate strategy, testing evidence, and labeling stay aligned before FDA review.