CENTRIX RIBBON TUBES— 510(k) K853282

Substantially Equivalent

Centrix, Inc.

FDA 510(k) clearance K853282 for CENTRIX RIBBON TUBES, Substantially Equivalent on 1985-08-23. Applicant: Centrix, Inc.. Device class: 1.

Clearance details

Applicant: Centrix, Inc.
Product code: Code EID
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 1985-08-05
Decision date: 1985-08-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stratford, 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.