FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
STIMULATOR, SONIC CONTROL (AS-1)
K Number: K760166
·
Decision Jul 20, 1976
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
5
Applicant Total
7
Review Days
14
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Basic Information
- Device Name
- STIMULATOR, SONIC CONTROL (AS-1)
- K Number
- K760166
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.5235
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Applicant
- Farrall Instruments, Inc.
- Date Received
- July 6, 1976
- Decision Date
- July 20, 1976
- Product Code
- HCB
- Advisory Committee
- Neurology
- Review Advisory Committee
- NE
- 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 |
|---|---|---|---|
| HCB | Device, Aversive Conditioning | FDA class 2 | Neurology |
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Other Clearances by Farrall Instruments, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K936115 | CAT-600 PENILE PLETHYSMOGRAPH | Jan 10, 1995 | Substantially Equivalent |
| K940128 | CAT-400UL PENILE PLETHYSMOGRAPH | Jan 10, 1995 | Substantially Equivalent |
| K821723 | BI-4520 DUAL IMPEDOMETER | Sep 15, 1982 | Substantially Equivalent |
| K821664 | PP-100, PERSONAL PERINEOMETER | Jul 13, 1982 | Substantially Equivalent |
| K792305 | A SLEEP ASSESSMENT DEVICE | Dec 20, 1979 | Substantially Equivalent |
| K781634 | VISUALAX | Oct 3, 1978 | Substantially Equivalent |