LIGHTSPEED CORDLESS ENDODONTIC HANDPIECE— 510(k) K050612

Name: FDA 510(k) clearance K050612
Creator: U.S. Food and Drug Administration
Published: 2005-05-04

Substantially Equivalent

Lightspeed Technology, Inc.

FDA 510(k) clearance K050612 for LIGHTSPEED CORDLESS ENDODONTIC HANDPIECE, Substantially Equivalent on 2005-05-04. Applicant: Lightspeed Technology, Inc.. Device class: 1.

Clearance details

Applicant: Lightspeed Technology, Inc.
Product code: Code EKX
Device class: Class 1
Regulation: 21 CFR 872.4200
Advisory panel: Dental
Date received: 2005-03-10
Decision date: 2005-05-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Antonio, TX, 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.