RION ELECTRO-PALATOGRAPH MODEL DP-01— 510(k) K802870

Name: FDA 510(k) clearance K802870
Creator: U.S. Food and Drug Administration
Published: 1980-12-17

Substantially Equivalent

Kindel & Anderson

FDA 510(k) clearance K802870 for RION ELECTRO-PALATOGRAPH MODEL DP-01, Substantially Equivalent on 1980-12-17. Applicant: Kindel & Anderson. Device class: Unclassified.

Clearance details

Applicant: Kindel & Anderson
Product code: Product code LEZ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1980-11-14
Decision date: 1980-12-17
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.