Last synced on 4 February 2023 at 10:33 pm

M32 IN-THE-EAR HEARING AID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913390
510(k) Type
Traditional
Applicant
PHILIPS HEARING INSTRUMENTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/1991
Days to Decision
28 days
Submission Type
Statement