CENTRAL VEIN CATHETERIZATION TRAY— 510(k) K852642

Name: FDA 510(k) clearance K852642
Creator: U.S. Food and Drug Administration
Published: 1986-01-16

Substantially Equivalent

Teleflexmedical, Inc.

FDA 510(k) clearance K852642 for CENTRAL VEIN CATHETERIZATION TRAY, Substantially Equivalent on 1986-01-16. Applicant: Teleflexmedical, Inc.. Device class: 1.

Clearance details

Applicant: Teleflexmedical, Inc.
Product code: Code FDZ
Device class: Class 1
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1985-06-21
Decision date: 1986-01-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jeffrey, NH, US

Download summary PDF View on FDA.gov ↗

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