510(k) K190767
K190767 is an FDA 510(k) premarket notification submitted by The Methodist Hospital Research Institute D/B/A Houston for the device "AnatomicAligner". The FDA issued a decision of Substantially Equivalent on Mar 16, 2020. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 16, 2020
- Date Received
- Mar 25, 2019
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Image Processing, Radiological
- Device Class
- Class II
- Regulation Number
- 892.2050
- Review Panel
- RA
- Submission Type
- 510(k)