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APNEALINK PRO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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