SIMUPLAN TREATMENT PLANNING SYSTEM— 510(k) K120551

Name: FDA 510(k) clearance K120551
Creator: U.S. Food and Drug Administration
Published: 2012-06-08

Substantially Equivalent

Simuplan S.L.

FDA 510(k) clearance K120551 for SIMUPLAN TREATMENT PLANNING SYSTEM, Substantially Equivalent on 2012-06-08. Applicant: Simuplan S.L.. Device class: 2.

Clearance details

Applicant: Simuplan S.L.
Product code: Code MUJ
Device class: Class 2
Regulation: 21 CFR 892.5050
Advisory panel: Radiology
Date received: 2012-02-23
Decision date: 2012-06-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rice Lake, WI, 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.