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BTE HEARING AID MULTIFOCUS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915614
510(k) Type
Traditional
Applicant
OPTICON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1992
Days to Decision
39 days
Submission Type
Statement