CEMENT-IT ALL PURPOSE, MODEL N97— 510(k) K060698

Name: FDA 510(k) clearance K060698
Creator: U.S. Food and Drug Administration
Published: 2006-05-10

Substantially Equivalent

Pentron Clinical Technologies

FDA 510(k) clearance K060698 for CEMENT-IT ALL PURPOSE, MODEL N97, Substantially Equivalent on 2006-05-10. 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: 2006-03-16
Decision date: 2006-05-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wallingford, CT, US

Download summary PDF View on FDA.gov ↗

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