Last synced on 22 September 2023 at 11:04 pm

BEHIND-THE-EAR HEARING AID MODEL 304 PP-AGC-I

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K891248
510(k) Type
Traditional
Applicant
SIEMENS HEARING INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1989
Days to Decision
21 days