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MOORVMS-LDF1 AND MOORVMS-LDF2 LASER DOPPLER PERFUSION AND TEMPERATURE MONITORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083082
510(k) Type
Traditional
Applicant
MOOR INSTRUMENTS LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/13/2009
Days to Decision
89 days
Submission Type
Summary

MOORVMS-LDF1 AND MOORVMS-LDF2 LASER DOPPLER PERFUSION AND TEMPERATURE MONITORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083082
510(k) Type
Traditional
Applicant
MOOR INSTRUMENTS LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/13/2009
Days to Decision
89 days
Submission Type
Summary