The following data is part of a premarket notification filed by Carina Medical Llc with the FDA for Int Contour.
Device ID | K212274 |
510k Number | K212274 |
Device Name: | INT Contour |
Classification | System, Planning, Radiation Therapy Treatment |
Applicant | Carina Medical LLC 1233 Litchfield Ln Lexington, KY 40513 |
Contact | Xue Feng |
Correspondent | Xue Feng Carina Medical LLC 1233 Litchfield Ln Lexington, KY 40513 |
Product Code | MUJ |
CFR Regulation Number | 892.5050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2021-07-20 |
Decision Date | 2022-04-08 |