510(k) K182533
K182533 is an FDA 510(k) premarket notification submitted by Pixxgen Corporation for the device "PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels". The FDA issued a decision of Substantially Equivalent on Oct 4, 2018. The device falls under product code MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager)), a Class II device regulated under 21 CFR 892.1680. Pixxgen Corporation has 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 4, 2018
- Date Received
- Sep 14, 2018
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Solid State X-Ray Imager (Flat Panel/Digital Imager)
- Device Class
- Class II
- Regulation Number
- 892.1680
- Review Panel
- RA
- Submission Type
- 510(k)