ULTRADENT PROD RETRACT CORD/ACCESSORY PRODUCT LINE— 510(k) K921601

Name: FDA 510(k) clearance K921601
Creator: U.S. Food and Drug Administration
Published: 1992-06-16

Substantially Equivalent

Ultradent Products, Inc.

FDA 510(k) clearance K921601 for ULTRADENT PROD RETRACT CORD/ACCESSORY PRODUCT LINE, Substantially Equivalent on 1992-06-16. Applicant: Ultradent Products, Inc.. Device class: 1.

Clearance details

Applicant: Ultradent Products, Inc.
Product code: Code JES
Device class: Class 1
Regulation: 21 CFR 872.6390
Advisory panel: Dental
Date received: 1992-04-03
Decision date: 1992-06-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, 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.