INTRAVENOUS INFUSION CONTROLLER— 510(k) K834106

Name: FDA 510(k) clearance K834106
Creator: U.S. Food and Drug Administration
Published: 1984-05-30

Substantially Equivalent

Cutter Laboratories, Inc.

FDA 510(k) clearance K834106 for INTRAVENOUS INFUSION CONTROLLER, Substantially Equivalent on 1984-05-30. Applicant: Cutter Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Cutter Laboratories, Inc.
Product code: Code LDR
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1983-11-29
Decision date: 1984-05-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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