510(k) K980383

MOOORLDI LASER DOPPLER IMAGER by Moor Instruments, Ltd. — Product Code DPT

K980383 is an FDA 510(k) premarket notification submitted by Moor Instruments, Ltd. for the device "MOOORLDI LASER DOPPLER IMAGER". The FDA issued a decision of Substantially Equivalent on April 30, 1998. 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
April 30, 1998
Date Received
February 2, 1998
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