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APNEALINK, MODEL 22302

Page Type
Cleared 510(K)
510(k) Number
K061405
510(k) Type
Traditional
Applicant
RESMED GERMANY INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2006
Days to Decision
67 days
Submission Type
Summary

APNEALINK, MODEL 22302

Page Type
Cleared 510(K)
510(k) Number
K061405
510(k) Type
Traditional
Applicant
RESMED GERMANY INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2006
Days to Decision
67 days
Submission Type
Summary