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PULSE OXIMETER MODEL P10

Page Type
Cleared 510(K)
510(k) Number
K100225
510(k) Type
Traditional
Applicant
MEDIANA CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/2011
Days to Decision
379 days
Submission Type
Summary

PULSE OXIMETER MODEL P10

Page Type
Cleared 510(K)
510(k) Number
K100225
510(k) Type
Traditional
Applicant
MEDIANA CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/2011
Days to Decision
379 days
Submission Type
Summary