FIBERFILL AGP— 510(k) K023818

Substantially Equivalent

Pentron Clinical Technologies

FDA 510(k) clearance K023818 for FIBERFILL AGP, Substantially Equivalent on 2003-04-03. Applicant: Pentron Clinical Technologies. Device class: 2.

Clearance details

Applicant: Pentron Clinical Technologies
Product code: Code KIF
Device class: Class 2
Regulation: 21 CFR 872.3820
Advisory panel: Dental
Date received: 2002-11-15
Decision date: 2003-04-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wallingford, CT, US

Download summary PDF View on FDA.gov ↗

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