510(k) K182208
K182208 is an FDA 510(k) premarket notification submitted by Siemens Healthcare GmbH for the device "syngo.via View&GO (Version VA10A)". The FDA issued a decision of Substantially Equivalent on Sep 7, 2018. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Siemens Healthcare GmbH has 31 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Sep 7, 2018
- Date Received
- Aug 15, 2018
- Clearance Type
- Abbreviated
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- System, Image Processing, Radiological
- Device Class
- Class II
- Regulation Number
- 892.2050
- Review Panel
- RA
- Submission Type
- 510(k)