DK*300 VOLUMETRIC INFUSION CONTROLLER— 510(k) K843254

Name: FDA 510(k) clearance K843254
Creator: U.S. Food and Drug Administration
Published: 1984-10-11

Substantially Equivalent

Deka Research & Development Corp.

FDA 510(k) clearance K843254 for DK*300 VOLUMETRIC INFUSION CONTROLLER, Substantially Equivalent on 1984-10-11. Applicant: Deka Research & Development Corp.. Device class: 2.

Clearance details

Applicant: Deka Research & Development Corp.
Product code: Code LDR
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1984-08-20
Decision date: 1984-10-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Manchester, NH, US

Download summary PDF View on FDA.gov ↗

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