ARM-A-FLOW INTRAVENOUS FLOW REGULATOR— 510(k) K842209

Name: FDA 510(k) clearance K842209
Creator: U.S. Food and Drug Administration
Published: 1984-12-04

Substantially Equivalent

Armour Pharmaceutical Co.

FDA 510(k) clearance K842209 for ARM-A-FLOW INTRAVENOUS FLOW REGULATOR, Substantially Equivalent on 1984-12-04. Applicant: Armour Pharmaceutical Co.. Device class: 2.

Clearance details

Applicant: Armour Pharmaceutical Co.
Product code: Code LDR
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1984-06-04
Decision date: 1984-12-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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