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AMPLAID A311 SERIES

Page Type
Cleared 510(K)
510(k) Number
K983712
510(k) Type
Traditional
Applicant
AMPLIFON S.P.A.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/1999
Days to Decision
83 days
Submission Type
Summary

AMPLAID A311 SERIES

Page Type
Cleared 510(K)
510(k) Number
K983712
510(k) Type
Traditional
Applicant
AMPLIFON S.P.A.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/1999
Days to Decision
83 days
Submission Type
Summary