FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

MOORFLPI-2 FULL-FIELD LASER PERFUSION IMAGER

K Number: K122943 · Decision Jan 3, 2013
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
47
Applicant Total
14
Review Days
101

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Basic Information

Device Name
MOORFLPI-2 FULL-FIELD LASER PERFUSION IMAGER
K Number
K122943
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2120
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Moor Instruments, Ltd.
Date Received
September 24, 2012
Decision Date
January 3, 2013
Product Code
DPT
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DPT Probe, Blood-Flow, Extravascular

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Other Clearances by Moor Instruments, Ltd.

K Number Device Name
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K132163 MOORLDLS-BI LASER DOPPLER BURNS IMAGER
K112826 NOORVMS-OXY TISSUE OXYGEN AND TEMPERTURE MONITOR
K102433 MOORVMS-PRES PRESSURE CUFF CONTROLLER
K083082 MOORVMS-LDF1 AND MOORVMS-LDF2 LASER DOPPLER PERFUSION AND TEMPERATURE MONITORS
K060976 MOORLD12-B1 LASER DOPPLER BURNS IMAGER
K063586 MOORFLPI FULL-FIELD LASER PERFUSION IMAGER
K063561 MOORLDLS LASER DOPPLER LINE SCANNER
K032841 MOORLDI INFRARED LASER DOPPLER IMAGER, MODEL MOORLD12-IR
K011070 DRT4 LASER DOPPLER PERFUSION AND TEMPERATURE MONITOR
Search all 14 clearances from Moor Instruments, Ltd. →