Last synced on 2 December 2022 at 11:04 pm

MODULAR HEARING DEVICE, MODEL S291

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K771762
510(k) Type
Traditional
Applicant
VICON INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/1977
Days to Decision
15 days