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APNEALINK

Page Type
Cleared 510(K)
510(k) Number
K070263
510(k) Type
Traditional
Applicant
RESMED GERMANY INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/2007
Days to Decision
140 days
Submission Type
Summary

APNEALINK

Page Type
Cleared 510(K)
510(k) Number
K070263
510(k) Type
Traditional
Applicant
RESMED GERMANY INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/2007
Days to Decision
140 days
Submission Type
Summary