510(k) K022741
K022741 is an FDA 510(k) premarket notification submitted by Nucletron Corporation for the device "SPOT PRO (220V), MODEL 131.099". The FDA issued a decision of Substantially Equivalent on October 24, 2002. The device falls under product code MUJ (System, Planning, Radiation Therapy Treatment), a Class II device regulated under 21 CFR 892.5050. Nucletron Corporation has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 24, 2002
- Date Received
- August 19, 2002
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Planning, Radiation Therapy Treatment
- Device Class
- Class II
- Regulation Number
- 892.5050
- Review Panel
- RA
- Submission Type