OTICON— 510(k) K821325
Substantially EquivalentOticon Corp.
FDA 510(k) clearance K821325 for OTICON, Substantially Equivalent on 1982-06-07. Applicant: Oticon Corp.. Device class: 1.
Clearance details
- Applicant
- Oticon Corp.
- 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
- Mchenry, IL, US
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