510(k) K032841

MOORLDI INFRARED LASER DOPPLER IMAGER, MODEL MOORLD12-IR by Moor Instruments, Ltd. — Product Code DPT

K032841 is an FDA 510(k) premarket notification submitted by Moor Instruments, Ltd. for the device "MOORLDI INFRARED LASER DOPPLER IMAGER, MODEL MOORLD12-IR". The FDA issued a decision of Substantially Equivalent on December 10, 2003. 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
December 10, 2003
Date Received
September 11, 2003
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