The following data is part of a premarket notification filed by Therapanacea with the FDA for Art-plan.
Device ID | K202700 |
510k Number | K202700 |
Device Name: | ART-Plan |
Classification | Radiological Image Processing Software For Radiation Therapy |
Applicant | TheraPanacea Pepiniere Cochin Paris Sante 29 Rue Du Faubourg Saint-Jacques Paris, FR 75014 |
Contact | Edwin Lindsay |
Correspondent | Edwin Lindsay TheraPanacea Pepiniere Cochin Paris Sante 29 Rue Du Faubourg Saint-Jacques Paris, FR 75014 |
Product Code | QKB |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2020-09-16 |
Decision Date | 2021-01-14 |