Last synced on 14 June 2024 at 11:05 pm

RESOUND PERSONAL HEARING SYSTEM ED3/S-E

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951375
510(k) Type
Traditional
Applicant
RESOUND CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/1995
Days to Decision
18 days
Submission Type
Summary