KLS Martin Individual Patient Solutions (IPS) Planning System— 510(k) K182789

Name: FDA 510(k) clearance K182789
Creator: U.S. Food and Drug Administration
Published: 2019-03-11

Substantially Equivalent

KLS-Martin L.P.

FDA 510(k) clearance K182789 for KLS Martin Individual Patient Solutions (IPS) Planning System, Substantially Equivalent on 2019-03-11. Applicant: KLS-Martin L.P.. Device class: 2.

Clearance details

Applicant: KLS-Martin L.P.
Product code: Code DZJ
Device class: Class 2
Regulation: 21 CFR 872.4120
Advisory panel: Dental
Date received: 2018-10-01
Decision date: 2019-03-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, 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.