ADVANCED DENTURE SYSTEM— 510(k) K780722

Name: FDA 510(k) clearance K780722
Creator: U.S. Food and Drug Administration
Published: 1978-05-26

Substantially Equivalent

Advanced Marketing Research Co.

FDA 510(k) clearance K780722 for ADVANCED DENTURE SYSTEM, Substantially Equivalent on 1978-05-26. Applicant: Advanced Marketing Research Co.. Device class: 2.

Clearance details

Applicant: Advanced Marketing Research Co.
Product code: Code EKO
Device class: Class 2
Regulation: 21 CFR 872.3600
Advisory panel: Dental
Date received: 1978-05-01
Decision date: 1978-05-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.