510(k) K151435
K151435 is an FDA 510(k) premarket notification submitted by Philips Medical Systems MR Finland for the device "MRCAT". The FDA issued a decision of Substantially Equivalent on Feb 25, 2016. The device falls under product code MUJ (System, Planning, Radiation Therapy Treatment), a Class II device regulated under 21 CFR 892.5050. Philips Medical Systems MR Finland has 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 25, 2016
- Date Received
- May 28, 2015
- 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)