REPROCESSED DIAMOND BURS— 510(k) K041978

Name: FDA 510(k) clearance K041978
Creator: U.S. Food and Drug Administration
Published: 2004-11-23

Substantially Equivalent

Alliance Medical Corp.

FDA 510(k) clearance K041978 for REPROCESSED DIAMOND BURS, Substantially Equivalent on 2004-11-23. Applicant: Alliance Medical Corp.. Device class: 2.

Clearance details

Applicant: Alliance Medical Corp.
Product code: Code NLN
Device class: Class 2
Regulation: 21 CFR 882.4310
Advisory panel: Neurology
Date received: 2004-07-23
Decision date: 2004-11-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Phoenix, AZ, US

Download summary PDF View on FDA.gov ↗

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