Last synced on 19 July 2024 at 11:05 pm

RESMED S8 PRIME CPAP SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033841
510(k) Type
Traditional
Applicant
RESMED LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/2004
Days to Decision
91 days
Submission Type
Summary

RESMED S8 PRIME CPAP SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033841
510(k) Type
Traditional
Applicant
RESMED LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/2004
Days to Decision
91 days
Submission Type
Summary