AMPLAID AM50— 510(k) K974235

Substantially Equivalent

Amplifon S.P.A.

FDA 510(k) clearance K974235 for AMPLAID AM50, Substantially Equivalent on 1998-02-10. Applicant: Amplifon S.P.A..

Clearance details

Applicant: Amplifon S.P.A.
Product code: Code ETY
Advisory panel: Ear, Nose, Throat
Date received: 1997-11-12
Decision date: 1998-02-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Deer Field, IL, US

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