Stimulator, Sonic Control (AS-1)
FDA 510(k) K760166 · Farrall Instruments, Inc.
510(k) numberK760166
Submission
- Device name
- Stimulator, Sonic Control (AS-1)
- Applicant
- Farrall Instruments, Inc.
Mchenry, IL, US - Received
- July 6, 1976
- Decision date
- July 20, 1976
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Other 510(k)s with product code HCB
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K911820 | Ged (Graduated Electronic DeceleratorHCB · Traditional | Behavior Research Institute, Inc. | 12/05/1994SE |
| K871158 | Sibis Remote ActuatorHCB · Traditional | Human Technologies, Inc. | 05/29/1987SE |
| K853178 | Sibis Self Injurious Behavior Inhibiting SystemHCB · Traditional | Oxford Medilog, Inc. | 02/28/1986SE |
| K820622 | Electrostimuli Aversion MachineHCB · Traditional | Michael R. Kiss | 04/09/1982SE |
| K790738 | HabitsabaterHCB · Traditional | Jackson Ent. | 06/20/1979SE |
More from Jackson Ent.
| 510(k) | Device | Decision |
|---|---|---|
| K940128 | CAT-400UL Penile PlethysmographLIL · Traditional | 01/10/1995SE |
| K936115 | CAT-600 Penile PlethysmographLIL · Traditional | 01/10/1995SE |
| K821723 | BI-4520 Dual Impedometer · Traditional | 09/15/1982SE |
| K821664 | PP-100, Personal PerineometerHIR · Traditional | 07/13/1982SE |
| K792305 | A Sleep Assessment DeviceLEL · Traditional | 12/20/1979SE |
| K781634 | VisualaxHCC · Traditional | 10/03/1978SE |
Questions and answers
When was Stimulator, Sonic Control (AS-1) cleared by the FDA?
Stimulator, Sonic Control (AS-1) (K760166) received a 510(k) decision of Substantially Equivalent on July 20, 1976, 14 days after the submission was received.
What is the product code of K760166?
The FDA product code is HCB – Device, Aversive Conditioning, a Class II (moderate risk) device regulated under 21 CFR 882.5235.