FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
EARETTE HEARING AID(BEHING THE EAR)
K Number: K810576
·
Decision Mar 17, 1981
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
1366
Applicant Total
57
Review Days
14
Basic Information
- Device Name
- EARETTE HEARING AID(BEHING THE EAR)
- K Number
- K810576
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 874.3300
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Applicant
- OTICON CORP.
- Date Received
- March 3, 1981
- Decision Date
- March 17, 1981
- 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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Other Clearances by OTICON CORP.
| K Number | Device Name | ||
|---|---|---|---|
| K963788 | PRIMOFOCUS COMPACT | Nov 27, 1996 | Substantially Equivalent |
| K932670 | OTICON MF | Aug 5, 1993 | Substantially Equivalent |
| K923388 | BTE HEARING AID OTICON MODEL: MULTIFOCUS POWER | Aug 6, 1992 | Substantially Equivalent |
| K923490 | BTE HEARING AID PERSONIC 410 | Aug 6, 1992 | Substantially Equivalent |
| K923491 | BTE HEARING AID PERSONIC 425 | Aug 6, 1992 | Substantially Equivalent |
| K905555 | A-ZILICONE | Jul 6, 1992 | Substantially Equivalent |
| K904673 | OTICAON BTE MODEL E34P | Nov 1, 1990 | Substantially Equivalent |
| K902559 | CUSTOM IN-THE-EAR HEARING AID OTICON MODEL: P | Jul 9, 1990 | Substantially Equivalent |
| K902351 | CUSTOM ITE HEARING AID MODELS C AND M | Jun 14, 1990 | Substantially Equivalent |
| K902352 | CUSTOM ITE HEARING AID MODEL: H | Jun 14, 1990 | Substantially Equivalent |