DEKA Infusion System, DEKA Administration Set— 510(k) K242693

Name: FDA 510(k) clearance K242693
Creator: U.S. Food and Drug Administration
Published: 2024-10-07

Substantially Equivalent

Deka 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. Device class: 2.

Clearance details

Applicant: Deka Research and Development Corporation
Product code: Code LDR
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 2024-09-09
Decision date: 2024-10-07
Decision: Substantially Equivalent
Clearance type: Special
Location: Manchester, NH, US

Download summary PDF View on FDA.gov ↗

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