510(k) K202293
K202293 is an FDA 510(k) premarket notification submitted by Sedecal., Sa. for the device "Radiographic System Challenge X". The FDA issued a decision of Substantially Equivalent on Oct 7, 2020. The device falls under product code KPR (System, X-Ray, Stationary), a Class II device regulated under 21 CFR 892.1680. Sedecal., Sa. has 25 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 7, 2020
- Date Received
- Aug 13, 2020
- Clearance Type
- Abbreviated
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, X-Ray, Stationary
- Device Class
- Class II
- Regulation Number
- 892.1680
- Review Panel
- RA
- Submission Type
- 510(k)