FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MAICO MA52
K Number: K971080
·
Decision Jun 6, 1997
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
234
Applicant Total
9
Review Days
73
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Basic Information
- Device Name
- MAICO MA52
- K Number
- K971080
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 874.1050
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Bernafon-Maico, Inc.
- Date Received
- March 25, 1997
- Decision Date
- June 6, 1997
- Product Code
- EWO
- 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 |
|---|---|---|---|
| EWO | Audiometer | FDA class 2 | Ear, Nose, Throat |
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Other Clearances by Bernafon-Maico, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K982723 | MAICO MA42 | Oct 28, 1998 | Substantially Equivalent |
| K981142 | MAICO MA53 | Apr 22, 1998 | Substantially Equivalent |
| K974211 | OPUS 2 - FULL CONCHA SERIES - ITE | Dec 15, 1997 | Substantially Equivalent |
| K974152 | OPUS 2 - COMPLETELY-IN-CANAL SERIES (CIC) | Dec 15, 1997 | Substantially Equivalent |
| K974069 | OPUS 2 - CANAL SERIES (ITC) | Dec 15, 1997 | Substantially Equivalent |
| K973948 | DUALINE 100 BTE | Oct 28, 1997 | Substantially Equivalent |
| K971158 | DUALINE 400 CIC | Jun 13, 1997 | Substantially Equivalent |
| K962275 | MAICO MA25 SERIES II WITH SPEECH | Sep 5, 1996 | Substantially Equivalent |