Last synced on 14 June 2024 at 11:05 pm

THE BREATHE EZ ANTI-SNORING DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022891
510(k) Type
Traditional
Applicant
D&S REDHAGE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/2003
Days to Decision
173 days
Submission Type
Summary

THE BREATHE EZ ANTI-SNORING DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022891
510(k) Type
Traditional
Applicant
D&S REDHAGE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/2003
Days to Decision
173 days
Submission Type
Summary