iiSure Infusion Set— 510(k) K261530
Substantially EquivalentDeka Research and Development
FDA 510(k) clearance K261530 for iiSure Infusion Set, Substantially Equivalent on 2026-06-03. Applicant: Deka Research and Development. Device class: 2.
Clearance details
- Applicant
- Deka Research and Development
- Product code
- Code FPA
- Device class
- Class 2
- Regulation
- 21 CFR 880.5440
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Manchester, NH, US
Recent devices under product code FPA
view all- K254123 — Ecomed Disposable Administration Sets
- K252543 — AMSafe 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)
- K251375 — PuraCath Firefly Needleless Connector IT (9005)
- K251257 — nSet+ Stabilization Set [6426733] +2 more
- K250325 — BD Alaris Pump Infusion Set
More clearances from Deka Research and Development
view allAdverse events under product code FPA
product code FPA- Death
- 95
- Injury
- 14,421
- Malfunction
- 125,815
- Other
- 30
- Total
- 140,361
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.