510(k) K231573
K231573 is an FDA 510(k) premarket notification submitted by Dosisoft SA for the device "ThinkQA (Edition 2)". The FDA issued a decision of Substantially Equivalent on January 18, 2024. The device falls under product code IYE (Accelerator, Linear, Medical), a Class II device regulated under 21 CFR 892.5050. Dosisoft SA has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 18, 2024
- Date Received
- May 31, 2023
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Accelerator, Linear, Medical
- Device Class
- Class II
- Regulation Number
- 892.5050
- Review Panel
- RA
- Submission Type