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MEDIAID PULSE OXIMETER M30 AND M34

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071610
510(k) Type
Traditional
Applicant
MEDIAID INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2007
Days to Decision
145 days
Submission Type
Summary

MEDIAID PULSE OXIMETER M30 AND M34

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071610
510(k) Type
Traditional
Applicant
MEDIAID INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2007
Days to Decision
145 days
Submission Type
Summary