TOURNIQUET/LATEX TOURNIQUET— 510(k) K830467

Name: FDA 510(k) clearance K830467
Creator: U.S. Food and Drug Administration
Published: 1983-03-31

Substantially Equivalent

Primeline Industries, Inc.

FDA 510(k) clearance K830467 for TOURNIQUET/LATEX TOURNIQUET, Substantially Equivalent on 1983-03-31. Applicant: Primeline Industries, Inc.. Device class: 1.

Clearance details

Applicant: Primeline Industries, Inc.
Product code: Code GAX
Device class: Class 1
Regulation: 21 CFR 878.5900
Advisory panel: General, Plastic Surgery
Date received: 1983-02-15
Decision date: 1983-03-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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