Last synced on 30 September 2022 at 11:05 pm

ITE HEARING AID, EARTECH/CUSTOM AID MODEL CA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882471
510(k) Type
Traditional
Applicant
EAR TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/1988
Days to Decision
72 days