WIDEX MODEL M1— 510(k) K853793
Substantially EquivalentWidex Hearing Aid Co., Inc.
FDA 510(k) clearance K853793 for WIDEX MODEL M1, Substantially Equivalent on 1985-12-02. 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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