MOORLD12-B1 Laser Doppler Burns Imager

FDA 510(k) K060976 · Moor Instruments, Ltd.

Substantially Equivalent

510(k) numberK060976

Submission

Device name
MOORLD12-B1 Laser Doppler Burns Imager
Applicant
Moor Instruments, Ltd.
Axminster, Devon, GB
Received
April 10, 2006
Decision date
March 27, 2007
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DPT – Probe, Blood-Flow, Extravascular
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2120
Specialty
Cardiovascular

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More from Moor Instruments, Ltd.

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K152749moorLDI2-IR Infrared laser Doppler imager, moorLDI2-HIR High Resolution Infrared laser…DPT · Traditional 05/12/2016SE
K132163Moorldls-Bi Laser Doppler Burns ImagerDPT · Traditional 01/29/2014SE
K122943MOORFLPI-2 Full-Field Laser Perfusion ImagerDPT · Traditional 01/03/2013SE
K112826Noorvms-Oxy Tissue Oxygen and Temperture MonitorMUD · Traditional 10/10/2012SE
K102433Moorvms-Pres Pressure Cuff ControllerDPW · Traditional 11/18/2010SE
K083082MOORVMS-LDF1 and MOORVMS-LDF2 Laser Doppler Perfusion and Temperature MonitorsGEX · Traditional 01/13/2009SE
K063586Moorflpi Full-Field Laser Perfusion ImagerDPT · Traditional 01/25/2007SE
K063561Moorldls Laser Doppler Line ScannerDPT · Traditional 01/19/2007SE
K032841Moorldi Infrared Laser Doppler Imager, Model MOORLD12-IRDPT · Traditional 12/10/2003SE
K011070DRT4 Laser Doppler Perfusion and Temperature MonitorGEX · Traditional 11/07/2001SE

Questions and answers

When was MOORLD12-B1 Laser Doppler Burns Imager cleared by the FDA?

MOORLD12-B1 Laser Doppler Burns Imager (K060976) received a 510(k) decision of Substantially Equivalent on March 27, 2007, 351 days after the submission was received.

What is the product code of K060976?

The FDA product code is DPT – Probe, Blood-Flow, Extravascular, a Class II (moderate risk) device regulated under 21 CFR 870.2120.