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POST-AURICULAR HEARING AID MODEL PE 600CHD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K844860
510(k) Type
Traditional
Applicant
PHONIC EAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1985
Days to Decision
103 days