INOMAX DS (DELIVERY SYSTEM)— 510(k) K090958

Name: FDA 510(k) clearance K090958
Creator: U.S. Food and Drug Administration
Published: 2009-06-18

Substantially Equivalent

Ino Therapeutics, LLC

FDA 510(k) clearance K090958 for INOMAX DS (DELIVERY SYSTEM), Substantially Equivalent on 2009-06-18. Applicant: Ino Therapeutics, LLC. Device class: 2.

Clearance details

Applicant: Ino Therapeutics, LLC
Product code: Code MNR
Device class: Class 2
Regulation: 21 CFR 868.2375
Advisory panel: Anesthesiology
Date received: 2009-04-06
Decision date: 2009-06-18
Decision: Substantially Equivalent
Clearance type: Special
Location: Madison, WI, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.