NORTEC CONNECTING TUBE SET— 510(k) K911865

Name: FDA 510(k) clearance K911865
Creator: U.S. Food and Drug Administration
Published: 1991-11-01

Substantially Equivalent

North American Sterilization & Packaging Co.

FDA 510(k) clearance K911865 for NORTEC CONNECTING TUBE SET, Substantially Equivalent on 1991-11-01. Applicant: North American Sterilization & Packaging Co.. Device class: 2.

Clearance details

Applicant: North American Sterilization & Packaging Co.
Product code: Code GAZ
Device class: Class 2
Regulation: 21 CFR 880.6740
Advisory panel: General Hospital
Date received: 1991-04-26
Decision date: 1991-11-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sparta, NJ, US

Download summary PDF View on FDA.gov ↗

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