MICRO-BOND HI-LIFE PROCELAIN & VIVERE— 510(k) K802235

Name: FDA 510(k) clearance K802235
Creator: U.S. Food and Drug Administration
Published: 1980-09-26

Substantially Equivalent

Howmedica Corp.

FDA 510(k) clearance K802235 for MICRO-BOND HI-LIFE PROCELAIN & VIVERE, Substantially Equivalent on 1980-09-26. Applicant: Howmedica Corp.. Device class: 2.

Clearance details

Applicant: Howmedica Corp.
Product code: Code EIH
Device class: Class 2
Regulation: 21 CFR 872.6660
Advisory panel: Dental
Date received: 1980-09-15
Decision date: 1980-09-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.