510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K980383Substantially Equivalent

Mooorldi Laser Doppler Imager

Moor Instruments Ltd., Axminster, Devon, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K980383 is the FDA 510(k) clearance record for MOOORLDI LASER DOPPLER IMAGER, a class II device, cleared for Moor Instruments, Ltd. on under FDA product code DPT (Probe, Blood-Flow, Extravascular). FDA records list 14 510(k) clearances for Moor Instruments, Ltd., from to . As of , FDA records show no recalls naming K980383.

Clearance record

Decision date
Received
(87 days to decision)
Product code
DPT Probe, Blood-Flow, Extravascular
Regulation
21 CFR 870.2120
Device class
Class II
Review panel
Cardiovascular
Applicant
Moor Instruments, Ltd. Millwey, Axminster, Devon, GB
510(k) summary
Summary
Third party review
No

Clearances, product code DPT

Trailing 12 months

FDA records hold no clearances under product code DPT in the trailing twelve months.

FDA records show no clearances under product code DPT in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DPT, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260