Last synced on 17 May 2024 at 11:06 pm

THE EQUALIZER AIRWAY DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K870501
510(k) Type
Traditional
Applicant
SLEEP RENEWAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1987
Days to Decision
28 days

THE EQUALIZER AIRWAY DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K870501
510(k) Type
Traditional
Applicant
SLEEP RENEWAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1987
Days to Decision
28 days