510(k) K090531
K090531 is an FDA 510(k) premarket notification submitted by Lifeline Software, Inc. for the device "RADCALC SOFTWARE, VERSION 6.0". The FDA issued a decision of Substantially Equivalent on May 27, 2009. The device falls under product code MUJ (System, Planning, Radiation Therapy Treatment), a Class II device regulated under 21 CFR 892.5050. Lifeline Software, Inc. has 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 27, 2009
- Date Received
- Feb 27, 2009
- Clearance Type
- Traditional
- 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
- 510(k)