XERAFIT— 510(k) K020062

Substantially Equivalent

Metalor Technologies USA

FDA 510(k) clearance K020062 for XERAFIT, Substantially Equivalent on 2002-02-14. Applicant: Metalor Technologies USA. Device class: 2.

Clearance details

Applicant: Metalor Technologies USA
Product code: Code EJH
Device class: Class 2
Regulation: 21 CFR 872.3710
Advisory panel: Dental
Date received: 2002-01-08
Decision date: 2002-02-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Attleborough, MA, US

Download summary PDF View on FDA.gov ↗

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