ULTRAPAK NEHA— 510(k) K010070

Name: FDA 510(k) clearance K010070
Creator: U.S. Food and Drug Administration
Published: 2001-03-15

Substantially Equivalent

Ultradent Products, Inc.

FDA 510(k) clearance K010070 for ULTRAPAK NEHA, Substantially Equivalent on 2001-03-15. Applicant: Ultradent Products, Inc.. Device class: Unclassified.

Clearance details

Applicant: Ultradent Products, Inc.
Product code: Code MVL
Device class: Unclassified
Advisory panel: Unknown
Date received: 2001-01-08
Decision date: 2001-03-15
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.