CERAMIBOND— 510(k) K802899

Substantially Equivalent

Zulauf, Inc.

FDA 510(k) clearance K802899 for CERAMIBOND, Substantially Equivalent on 1980-12-19. Applicant: Zulauf, Inc.. Device class: 2.

Clearance details

Applicant: Zulauf, Inc.
Product code: Code DYW
Device class: Class 2
Regulation: 21 CFR 872.5470
Advisory panel: Dental
Date received: 1980-11-17
Decision date: 1980-12-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, 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.