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N-600X WITH SPD, OXIMAX N-600X

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083325
510(k) Type
Traditional
Applicant
COVIDIEN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/2009
Days to Decision
117 days
Submission Type
Summary

N-600X WITH SPD, OXIMAX N-600X

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083325
510(k) Type
Traditional
Applicant
COVIDIEN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/2009
Days to Decision
117 days
Submission Type
Summary