ULTRA-BLEND PLUS— 510(k) K970113

Substantially Equivalent

Ultradent Products, Inc.

FDA 510(k) clearance K970113 for ULTRA-BLEND PLUS, Substantially Equivalent on 1997-04-02. Applicant: Ultradent Products, Inc.. Device class: 2.

Clearance details

Applicant: Ultradent Products, Inc.
Product code: Code EJK
Device class: Class 2
Regulation: 21 CFR 872.3250
Advisory panel: Dental
Date received: 1997-01-13
Decision date: 1997-04-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: South Jordan, UT, 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.