MIN-IDENTOFLEX— 510(k) K873002

Substantially Equivalent

Centrix, Inc.

FDA 510(k) clearance K873002 for MIN-IDENTOFLEX, Substantially Equivalent on 1987-08-17. Applicant: Centrix, Inc.. Device class: 1.

Clearance details

Applicant: Centrix, Inc.
Product code: Code EHJ
Device class: Class 1
Regulation: 21 CFR 872.6010
Advisory panel: Dental
Date received: 1987-08-04
Decision date: 1987-08-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milford, 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.