SIMUPLAN TREATMENT PLANNING SYSTEM, MODEL V. 7.5— 510(k) K030821

Name: FDA 510(k) clearance K030821
Creator: U.S. Food and Drug Administration
Published: 2003-09-17

Substantially Equivalent

Simuplan S.L.

FDA 510(k) clearance K030821 for SIMUPLAN TREATMENT PLANNING SYSTEM, MODEL V. 7.5, Substantially Equivalent on 2003-09-17. 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: 2003-03-14
Decision date: 2003-09-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: La Eliana Valencia, ES

Download summary PDF View on FDA.gov ↗

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