510(k) K790738
- Device
- HABITSABATER
- Applicant
- JACKSON ENT.
- 510(k) number
- K790738
- Product code
- HCB
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1979-06-20
- Date received
- 1979-04-16
- Regulation
- 882.5235
- Classification name
- Device, Aversive Conditioning
- Medical specialty
- Neurology
- Review panel
- Neurology
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 1222743
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code HCB #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K911820 | GED (GRADUATED ELECTRONIC DECELERATOR | Behavior Research Institute, Inc. | 1994-12-05 |
| K871158 | SIBIS REMOTE ACTUATOR | Human Technologies, Inc. | 1987-05-29 |
| K853178 | SIBIS SELF INJURIOUS BEHAVIOR INHIBITING SYSTEM | Oxford Medilog, Inc. | 1986-02-28 |
| K820622 | ELECTROSTIMULI AVERSION MACHINE | Michael R. Kiss | 1982-04-09 |
| K760166 | STIMULATOR, SONIC CONTROL (AS-1) | Farrall Instruments, Inc. | 1976-07-20 |
Legacy Summary#
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FDA Review#
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