510(k) K221677
K221677 is an FDA 510(k) premarket notification submitted by Fujifilm Corporation for the device "Synapse 3D Base Tools v6.6". The FDA issued a decision of Substantially Equivalent on Nov 10, 2022. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Fujifilm Corporation has 69 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Nov 10, 2022
- Date Received
- Jun 9, 2022
- 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)