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

MOOR LASER BLOOD FLOW MONITOR MBF3

K Number: K905232 · Decision Jan 11, 1991
Classifications
1
FEI Numbers
478
Registration Numbers
480
Same Product Code
2867
Applicant Total
14
Review Days
52

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MOOR LASER BLOOD FLOW MONITOR MBF3
K Number
K905232
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Moor Instruments, Ltd.
Date Received
November 20, 1990
Decision Date
January 11, 1991
Product Code
GEX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEX Powered Laser Surgical Instrument

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GEX), ordered by most recent decision date.

View all

Other Clearances by Moor Instruments, Ltd.

K Number Device Name
K152749 moorLDI2-IR Infrared laser Doppler imager, moorLDI2-HIR High Resolution Infrared laser Doppler imager, moorLDI2-VR Visible Red laser Doppler imager
K132163 MOORLDLS-BI LASER DOPPLER BURNS IMAGER
K122943 MOORFLPI-2 FULL-FIELD LASER PERFUSION 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
Search all 14 clearances from Moor Instruments, Ltd. →