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CLEARTONE MODEL-1 & 2 HEARING AIDS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K780459
510(k) Type
Traditional
Applicant
CLEARTONE CUSTOM HEARING INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/1978
Days to Decision
7 days