510(k) K234068

Device
ART-Plan (v.2.2.0)
Applicant
Therapanacea Sas
510(k) number
K234068
Product code
MUJ
Decision
Substantially Equivalent (SESE)
Decision date
2024-04-22
Date received
2023-12-22
Regulation
892.5050
Classification name
System, Planning, Radiation Therapy Treatment
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Bhairavi Ajachandra
Address
7 Bis Blvd. Bourdon Paris FR 75004 75004

FDA Registration Numbers

Source Documents

510(k) summary PDF

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