ROBINSON MEDSURG QUICKSCREW RACK— 510(k) K093800

Name: FDA 510(k) clearance K093800
Creator: U.S. Food and Drug Administration
Published: 2010-06-16

Substantially Equivalent

Robinson Medsurg, LLC

FDA 510(k) clearance K093800 for ROBINSON MEDSURG QUICKSCREW RACK, Substantially Equivalent on 2010-06-16. Applicant: Robinson Medsurg, LLC. Device class: 2.

Clearance details

Applicant: Robinson Medsurg, LLC
Product code: Code KCT
Device class: Class 2
Regulation: 21 CFR 880.6850
Advisory panel: General Hospital
Date received: 2009-12-10
Decision date: 2010-06-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lone Tree, CO, US

Download summary PDF View on FDA.gov ↗

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