PROFESSIONAL MODEL 7525 DELIVERY SYSTEM— 510(k) K882759

Name: FDA 510(k) clearance K882759
Creator: U.S. Food and Drug Administration
Published: 1988-08-12

Substantially Equivalent

Viadent

FDA 510(k) clearance K882759 for PROFESSIONAL MODEL 7525 DELIVERY SYSTEM, Substantially Equivalent on 1988-08-12. Applicant: Viadent. Device class: 1.

Clearance details

Applicant: Viadent
Product code: Code EFS
Device class: Class 1
Regulation: 21 CFR 872.6510
Advisory panel: Dental
Date received: 1988-07-05
Decision date: 1988-08-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Collins, CO, 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.