510(k) K063586

MOORFLPI FULL-FIELD LASER PERFUSION IMAGER by Moor Instruments, Ltd. — Product Code DPT

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