SAFETY RELEASE ARCH BAR KIT— 510(k) K031207

Name: FDA 510(k) clearance K031207
Creator: U.S. Food and Drug Administration
Published: 2003-07-15

Substantially Equivalent

Casey Surgical, LLC

FDA 510(k) clearance K031207 for SAFETY RELEASE ARCH BAR KIT, Substantially Equivalent on 2003-07-15. Applicant: Casey Surgical, LLC. Device class: 2.

Clearance details

Applicant: Casey Surgical, LLC
Product code: Code DYX
Device class: Class 2
Regulation: 21 CFR 872.4600
Advisory panel: Dental
Date received: 2003-04-16
Decision date: 2003-07-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lee'S Summit, MO, US

Download summary PDF View on FDA.gov ↗

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