Last synced on 20 December 2024 at 11:05 pm

AMPLAID 460

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971747
510(k) Type
Traditional
Applicant
AMPLIFON S.P.A.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/1997
Days to Decision
85 days
Submission Type
Summary

AMPLAID 460

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971747
510(k) Type
Traditional
Applicant
AMPLIFON S.P.A.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/1997
Days to Decision
85 days
Submission Type
Summary