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LUCON M-SERIES PATIENT MONITOR, MODELS M20 AND M30

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100217
510(k) Type
Traditional
Applicant
MEDIANA CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/2010
Days to Decision
134 days
Submission Type
Summary

LUCON M-SERIES PATIENT MONITOR, MODELS M20 AND M30

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100217
510(k) Type
Traditional
Applicant
MEDIANA CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/2010
Days to Decision
134 days
Submission Type
Summary