Last synced on 14 November 2025 at 11:06 pm

APNEALINK PRO

Page Type
Cleared 510(K)
510(k) Number
K131932
510(k) Type
Traditional
Applicant
RESMED GERMANY INC.
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
11/8/2013
Days to Decision
134 days
Submission Type
Summary

APNEALINK PRO

Page Type
Cleared 510(K)
510(k) Number
K131932
510(k) Type
Traditional
Applicant
RESMED GERMANY INC.
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
11/8/2013
Days to Decision
134 days
Submission Type
Summary