DENTINSENSE B/C— 510(k) K965138

Substantially Equivalent

Centrix, Inc.

FDA 510(k) clearance K965138 for DENTINSENSE B/C, Substantially Equivalent on 1997-02-14. Applicant: Centrix, Inc.. Device class: 2.

Clearance details

Applicant: Centrix, Inc.
Product code: Code KLE
Device class: Class 2
Regulation: 21 CFR 872.3200
Advisory panel: Dental
Date received: 1996-12-23
Decision date: 1997-02-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shelton, 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.