Last synced on 9 June 2023 at 11:04 pm

POST-AURICULAR HEARING AID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K840359
510(k) Type
Traditional
Applicant
PHONIC EAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/1984
Days to Decision
26 days