510(k) K213370
K213370 is an FDA 510(k) premarket notification submitted by Ptw-Freiburg Physikalisch-Technische-Werkstaetten for the device "VERIQA". The FDA issued a decision of Substantially Equivalent on Mar 30, 2022. The device falls under product code IYE (Accelerator, Linear, Medical), a Class II device regulated under 21 CFR 892.5050. Ptw-Freiburg Physikalisch-Technische-Werkstaetten has 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 30, 2022
- Date Received
- Oct 12, 2021
- 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
- 510(k)