TRIONOMER— 510(k) K022150

Substantially Equivalent

Pentron Clinical Technologies

FDA 510(k) clearance K022150 for TRIONOMER, Substantially Equivalent on 2002-08-21. Applicant: Pentron Clinical Technologies. Device class: 2.

Clearance details

Applicant: Pentron Clinical Technologies
Product code: Code EMA
Device class: Class 2
Regulation: 21 CFR 872.3275
Advisory panel: Dental
Date received: 2002-07-02
Decision date: 2002-08-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wallingford, CT, 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.