PROVILINK— 510(k) K950060

Substantially Equivalent

Ivoclar North America, Inc.

FDA 510(k) clearance K950060 for PROVILINK, Substantially Equivalent on 1995-02-10. Applicant: Ivoclar North America, Inc..

Clearance details

Applicant: Ivoclar North America, Inc.
Product code: Code EMA
Advisory panel: Dental
Date received: 1995-01-06
Decision date: 1995-02-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Amherst, NY, US

Download summary PDF View on FDA.gov ↗

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