510(k) K260482
K260482 is an FDA 510(k) premarket notification submitted by Jpi Healthcare Co, Ltd. for the device "DRE Duo". The FDA issued a decision of Substantially Equivalent on June 15, 2026. The device falls under product code KPR (System, X-Ray, Stationary), a Class II device regulated under 21 CFR 892.1680. Jpi Healthcare Co, Ltd. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 15, 2026
- Date Received
- February 13, 2026
- Clearance Type
- Traditional
- 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