510(k) K252992
K252992 is an FDA 510(k) premarket notification submitted by Philips Healthcare (Suzhou) Co., Ltd. for the device "CT Rembra RT; CT Areta RT; CT Rembra". The FDA issued a decision of Substantially Equivalent on March 23, 2026. The device falls under product code JAK (System, X-Ray, Tomography, Computed), a Class II device regulated under 21 CFR 892.1750. Philips Healthcare (Suzhou) Co., Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 23, 2026
- Date Received
- September 18, 2025
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, X-Ray, Tomography, Computed
- Device Class
- Class II
- Regulation Number
- 892.1750
- Review Panel
- RA
- Submission Type