SPIRTIUS CUFF INFLATION SYRINGE— 510(k) K112915

Name: FDA 510(k) clearance K112915
Creator: U.S. Food and Drug Administration
Published: 2012-05-25

Substantially Equivalent

Spiritus Technologies, LLC

FDA 510(k) clearance K112915 for SPIRTIUS CUFF INFLATION SYRINGE, Substantially Equivalent on 2012-05-25. Applicant: Spiritus Technologies, LLC. Device class: 2.

Clearance details

Applicant: Spiritus Technologies, LLC
Product code: Code BSK
Device class: Class 2
Regulation: 21 CFR 868.5750
Advisory panel: Anesthesiology
Date received: 2011-10-03
Decision date: 2012-05-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lenexa, KS, US

Download summary PDF View on FDA.gov ↗

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