510(k) K840226
K840226 is an FDA 510(k) premarket notification submitted by Medicor USA , Ltd. for the device "MOTOR TILTED EXAM. TABLE UV-56". The FDA issued a decision of Substantially Equivalent on March 16, 1984. The device falls under product code IXR (Table, Radiographic, Tilting), a Class II device regulated under 21 CFR 892.1980. Medicor USA , Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 16, 1984
- Date Received
- January 19, 1984
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Table, Radiographic, Tilting
- Device Class
- Class II
- Regulation Number
- 892.1980
- Review Panel
- RA
- Submission Type