SONATA MICRO HYBRID COMPOSITE— 510(k) K020555

Name: FDA 510(k) clearance K020555
Creator: U.S. Food and Drug Administration
Published: 2002-04-22

Substantially Equivalent

Pentron Laboratory Technologies

FDA 510(k) clearance K020555 for SONATA MICRO HYBRID COMPOSITE, Substantially Equivalent on 2002-04-22. Applicant: Pentron Laboratory Technologies. Device class: 2.

Clearance details

Applicant: Pentron Laboratory Technologies
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 2002-02-20
Decision date: 2002-04-22
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.