AMPLAID AM50— 510(k) K974235
Substantially EquivalentAmplifon S.P.A.
FDA 510(k) clearance K974235 for AMPLAID AM50, Substantially Equivalent on 1998-02-10. Applicant: Amplifon S.P.A.. Device class: 2.
Clearance details
- Applicant
- Amplifon S.P.A.
- Product code
- Code ETY
- Device class
- Class 2
- Regulation
- 21 CFR 874.1090
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Deer Field, IL, US
Recent devices under product code ETY
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