510(k) K210982
K210982 is an FDA 510(k) premarket notification submitted by Ge Medical Systems, LLC for the device "AMX Navigate". The FDA issued a decision of Substantially Equivalent on Apr 28, 2021. The device falls under product code IZL (System, X-Ray, Mobile), a Class II device regulated under 21 CFR 892.1720. Ge Medical Systems, LLC has 328 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 28, 2021
- Date Received
- Apr 1, 2021
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, X-Ray, Mobile
- Device Class
- Class II
- Regulation Number
- 892.1720
- Review Panel
- RA
- Submission Type
- 510(k)