VIANOX DELIVERY SYSTEM, MODEL I— 510(k) K023014

Name: FDA 510(k) clearance K023014
Creator: U.S. Food and Drug Administration
Published: 2003-08-14

Substantially Equivalent

Pulmonox Medical, Inc.

FDA 510(k) clearance K023014 for VIANOX DELIVERY SYSTEM, MODEL I, Substantially Equivalent on 2003-08-14. Applicant: Pulmonox Medical, Inc.. Device class: 2.

Clearance details

Applicant: Pulmonox Medical, Inc.
Product code: Code MRP
Device class: Class 2
Regulation: 21 CFR 868.2380
Advisory panel: Anesthesiology
Date received: 2002-09-10
Decision date: 2003-08-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Edmonton, Ab, CA

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