Last synced on 14 November 2025 at 11:06 pm

OXYGEN DIVERTER VALVE

Page Type
Cleared 510(K)
510(k) Number
K033914
510(k) Type
Traditional
Applicant
RESMED LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/2004
Days to Decision
126 days
Submission Type
Summary

OXYGEN DIVERTER VALVE

Page Type
Cleared 510(K)
510(k) Number
K033914
510(k) Type
Traditional
Applicant
RESMED LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/2004
Days to Decision
126 days
Submission Type
Summary