Last synced on 30 September 2022 at 11:05 pm

RESOUND PERSONAL HEARING SYSTEMS EDR ENCORE SERIES MODELS EDR-E, EDR-ES, EDR-EV, & EDR-P1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960680
510(k) Type
Traditional
Applicant
RESOUND CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1996
Days to Decision
50 days
Submission Type
Summary