Last synced on 14 November 2025 at 11:06 pm

RESCAN

Page Type
Cleared 510(K)
510(k) Number
K034033
510(k) Type
Traditional
Applicant
RESMED LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/2004
Days to Decision
128 days
Submission Type
Summary

RESCAN

Page Type
Cleared 510(K)
510(k) Number
K034033
510(k) Type
Traditional
Applicant
RESMED LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/2004
Days to Decision
128 days
Submission Type
Summary