ELECTROSTIMULI AVERSION MACHINE
FDA 510(k) clearance K820622 · decided 1982-04-09
Clearance details
- K-number
- K820622
- Device name
- ELECTROSTIMULI AVERSION MACHINE
- Applicant
- Michael R. Kiss
- Decision
- Substantially Equivalent
- Date received
- 1982-03-08
- Decision date
- 1982-04-09
- Days to decision
- 32 days
- Clearance type
- Traditional
- Product code
- HCB
- Device class
- 2
- Regulation number
- 882.5235
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| GED (GRADUATED ELECTRONIC DECELERATOR (K911820) | Behavior Research Institute, Inc. | 1994-12-05 |
| SIBIS REMOTE ACTUATOR (K871158) | Human Technologies, Inc. | 1987-05-29 |
| SIBIS SELF INJURIOUS BEHAVIOR INHIBITING SYSTEM (K853178) | Oxford Medilog, Inc. | 1986-02-28 |
| HABITSABATER (K790738) | Jackson Ent. | 1979-06-20 |
| STIMULATOR, SONIC CONTROL (AS-1) (K760166) | Farrall Instruments, Inc. | 1976-07-20 |
Recalls involving this device
No recalls on record reference this clearance.