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AMPLAID MK12

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971740
510(k) Type
Traditional
Applicant
AMPLIFON S.P.A.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/1998
Days to Decision
308 days
Submission Type
Summary

AMPLAID MK12

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971740
510(k) Type
Traditional
Applicant
AMPLIFON S.P.A.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/1998
Days to Decision
308 days
Submission Type
Summary