The following data is part of a premarket notification filed by Mim Software Inc. with the FDA for Contour Protegeai.
Device ID | K210632 |
510k Number | K210632 |
Device Name: | Contour ProtegeAI |
Classification | Radiological Image Processing Software For Radiation Therapy |
Applicant | MIM Software Inc. 25800 Science Park Drive - Suite 180 Cleveland, OH 44122 |
Contact | Lynn Hanigan |
Correspondent | Lynn Hanigan MIM Software Inc. 25800 Science Park Drive - Suite 180 Cleveland, OH 44122 |
Product Code | QKB |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2021-03-03 |
Decision Date | 2021-10-20 |