Last synced on 25 January 2026 at 3:41 am

155 PP AGC-I

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940608
510(k) Type
Traditional
Applicant
DANAVOX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/1994
Days to Decision
79 days
Submission Type
Statement

155 PP AGC-I

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940608
510(k) Type
Traditional
Applicant
DANAVOX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/1994
Days to Decision
79 days
Submission Type
Statement