Last synced on 25 November 2022 at 11:04 pm

SUPER-SIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940164
510(k) Type
Traditional
Applicant
FINETONE HEARING INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/29/1994
Days to Decision
174 days
Submission Type
Statement