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RESTRAXX DATA CENTRE, MODEL R10

Page Type
Cleared 510(K)
510(k) Number
K070746
510(k) Type
Traditional
Applicant
RESMED LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/2007
Days to Decision
116 days
Submission Type
Summary

RESTRAXX DATA CENTRE, MODEL R10

Page Type
Cleared 510(K)
510(k) Number
K070746
510(k) Type
Traditional
Applicant
RESMED LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/2007
Days to Decision
116 days
Submission Type
Summary