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MOOR LASER BLOOD FLOW MONITOR MBF3D

Page Type
Cleared 510(K)
510(k) Number
K905233
510(k) Type
Traditional
Applicant
MOOR INSTRUMENTS LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/11/1991
Days to Decision
52 days

MOOR LASER BLOOD FLOW MONITOR MBF3D

Page Type
Cleared 510(K)
510(k) Number
K905233
510(k) Type
Traditional
Applicant
MOOR INSTRUMENTS LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/11/1991
Days to Decision
52 days