PERIOGENIX— 510(k) K083516

Substantially Equivalent

Oroscience, Inc.

FDA 510(k) clearance K083516 for PERIOGENIX, Substantially Equivalent on 2009-02-20. Applicant: Oroscience, Inc.. Device class: 2.

Clearance details

Applicant: Oroscience, Inc.
Product code: Code EMA
Device class: Class 2
Regulation: 21 CFR 872.3275
Advisory panel: Dental
Date received: 2008-11-26
Decision date: 2009-02-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Attleboro, MA, 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.