PERIOFLEX TIP— 510(k) K923711

Substantially Equivalent

Novadent, Ltd.

FDA 510(k) clearance K923711 for PERIOFLEX TIP, Substantially Equivalent on 1994-05-16. Applicant: Novadent, Ltd.. Device class: 1.

Clearance details

Applicant: Novadent, Ltd.
Product code: Code EFS
Device class: Class 1
Regulation: 21 CFR 872.6510
Advisory panel: Dental
Date received: 1992-07-27
Decision date: 1994-05-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jerusalem, IL

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.