DEKA Infusion System, DEKA Administration Set— 510(k) K242693
Substantially EquivalentDeka Research and Development Corporation
FDA 510(k) clearance K242693 for DEKA Infusion System, DEKA Administration Set, Substantially Equivalent on 2024-10-07. Applicant: Deka Research and Development Corporation.
Clearance details
- Applicant
- Deka Research and Development Corporation
- Product code
- Code LDR
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Manchester, NH, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.