FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
RASTRONICS CCI 10/3 HEARING AID ANALYSIS
K Number: K902252
·
Decision Sep 12, 1990
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
45
Applicant Total
5
Review Days
114
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Basic Information
- Device Name
- RASTRONICS CCI 10/3 HEARING AID ANALYSIS
- K Number
- K902252
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 874.3310
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Applicant
- Rastronics USA, Inc.
- Date Received
- May 21, 1990
- Decision Date
- September 12, 1990
- Product Code
- ETW
- 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 |
|---|---|---|---|
| ETW | Calibrator, Hearing Aid / Earphone And Analysis Systems | FDA class 2 | Ear, Nose, Throat |
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Other Clearances by Rastronics USA, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K902244 | RASTRONICS CCI 8 | Oct 5, 1990 | Substantially Equivalent |
| K902287 | RASTRONICS PORTAREM 20 | Aug 9, 1990 | Substantially Equivalent |
| K890864 | HANDTYMP SCREENER MODEL 2000 + 2002 REMOTE TRANS. | Jun 21, 1989 | Substantially Equivalent |
| K853320 | FREQUENCY RESPONSE ANALYZER COMPUTER SYS CCI-10 | Sep 27, 1985 | Substantially Equivalent |