Last synced on 20 May 2022 at 11:05 pm

RESSCAN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050775
510(k) Type
Traditional
Applicant
RESMED LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/2005
Days to Decision
43 days
Submission Type
Summary

RESSCAN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050775
510(k) Type
Traditional
Applicant
RESMED LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/2005
Days to Decision
43 days
Submission Type
Summary