FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ELECTROSTIMULI AVERSION MACHINE
K Number: K820622
·
Decision Apr 9, 1982
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
5
Applicant Total
1
Review Days
32
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Basic Information
- Device Name
- ELECTROSTIMULI AVERSION MACHINE
- K Number
- K820622
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.5235
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Applicant
- Michael R. Kiss
- Date Received
- March 8, 1982
- Decision Date
- April 9, 1982
- 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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