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PULSE OXIMETER MODEL P10

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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