AMENDMENTS TO MULTIFOCUS— 510(k) K951002
Substantially EquivalentOticon A/S
FDA 510(k) clearance K951002 for AMENDMENTS TO MULTIFOCUS, Substantially Equivalent on 1995-09-18. Applicant: Oticon A/S. Device class: 1.
Clearance details
- Applicant
- Oticon A/S
- 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
- Thisted, DK
Recent devices under product code ESD
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