DEKA Infusion System, DEKA Administration Set— 510(k) K232316
Substantially EquivalentDeka Research and Development
FDA 510(k) clearance K232316 for DEKA Infusion System, DEKA Administration Set, Substantially Equivalent on 2024-03-01. Applicant: Deka Research and Development. Device class: 2.
Clearance details
- Applicant
- Deka Research and Development
- Product code
- Code LDR
- Device class
- Class 2
- Regulation
- 21 CFR 880.5725
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Manchester, NH, US
Recent devices under product code LDR
view allMore clearances from Deka Research and Development
view allData sourced from openFDA. This site is unofficial and independent of the FDA.