WIDEX HEARING AID MODEL C1— 510(k) K880273
Substantially EquivalentWidex Hearing Aid Co., Inc.
FDA 510(k) clearance K880273 for WIDEX HEARING AID MODEL C1, Substantially Equivalent on 1988-03-14. Applicant: Widex Hearing Aid Co., Inc.. Device class: 1.
Clearance details
- Applicant
- Widex Hearing Aid Co., Inc.
- Product code
- Code ESD
- Device class
- Class 1
- Regulation
- 21 CFR 874.3300
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Long Island City, NY, US
Recent devices under product code ESD
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