FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
WIDEX HEARING AID #'S A12+T & A12+H
K Number: K802307
·
Decision Oct 10, 1980
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
1366
Applicant Total
4
Review Days
17
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Basic Information
- Device Name
- WIDEX HEARING AID #'S A12+T & A12+H
- K Number
- K802307
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 874.3300
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Applicant
- Hearing Aid Co.
- Date Received
- September 23, 1980
- Decision Date
- October 10, 1980
- Product Code
- ESD
- Advisory Committee
- Ear, Nose, Throat
- Review Advisory Committee
- EN
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| ESD | Hearing Aid, Air-Conduction, Prescription | FDA class 1 | Ear, Nose, Throat |
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