510(k) K202360
K202360 is an FDA 510(k) premarket notification submitted by Ziehm Imaging GmbH for the device "Ziehm Vision RFD 3D". The FDA issued a decision of Substantially Equivalent on September 16, 2020. The device falls under product code OWB (Interventional Fluoroscopic X-Ray System), a Class II device regulated under 21 CFR 892.1650. Ziehm Imaging GmbH has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 16, 2020
- Date Received
- August 19, 2020
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Interventional Fluoroscopic X-Ray System
- Device Class
- Class II
- Regulation Number
- 892.1650
- Review Panel
- RA
- Submission Type
Interventional fluoroscopy