510(k) K063586
K063586 is an FDA 510(k) premarket notification submitted by Moor Instruments, Ltd. for the device "MOORFLPI FULL-FIELD LASER PERFUSION IMAGER". The FDA issued a decision of Substantially Equivalent on January 25, 2007. The device falls under product code DPT (Probe, Blood-Flow, Extravascular), a Class II device regulated under 21 CFR 870.2120. Moor Instruments, Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 25, 2007
- Date Received
- December 1, 2006
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Probe, Blood-Flow, Extravascular
- Device Class
- Class II
- Regulation Number
- 870.2120
- Review Panel
- CV
- Submission Type