IMPLANT CENTER 2— 510(k) K091252

Substantially Equivalent

Satelec

FDA 510(k) clearance K091252 for IMPLANT CENTER 2, Substantially Equivalent on 2009-07-22. Applicant: Satelec. Device class: 2.

Clearance details

Applicant: Satelec
Product code: Code DZI
Device class: Class 2
Regulation: 21 CFR 872.4120
Advisory panel: Dental
Date received: 2009-04-29
Decision date: 2009-07-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mt. Laurel, NJ, 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.