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RESOUND PERSONAL HEARING SYSTEM MODELS ED3A & ED3A/S W/REMONTE CONTROL OPTION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951379
510(k) Type
Traditional
Applicant
RESOUND CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/1995
Days to Decision
31 days
Submission Type
Summary