FIBERFILL SGP— 510(k) K023819

Substantially Equivalent

Pentron Clinical Technologies

FDA 510(k) clearance K023819 for FIBERFILL SGP, Substantially Equivalent on 2003-03-26. Applicant: Pentron Clinical Technologies. Device class: 1.

Clearance details

Applicant: Pentron Clinical Technologies
Product code: Code EKM
Device class: Class 1
Regulation: 21 CFR 872.3850
Advisory panel: Dental
Date received: 2002-11-15
Decision date: 2003-03-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wallingford, CT, US

Download summary PDF View on FDA.gov ↗

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