FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
STIMPEN
K Number: K822139
·
Decision Sep 13, 1982
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
62
Applicant Total
5
Review Days
56
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Basic Information
- Device Name
- STIMPEN
- K Number
- K822139
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.2775
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Neuro Technology
- Date Received
- July 19, 1982
- Decision Date
- September 13, 1982
- Product Code
- BXN
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- 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 |
|---|---|---|---|
| BXN | Stimulator, Nerve, Battery-Powered | FDA class 2 | Anesthesiology |
Similar 510(k) Clearances
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STIMPOD ST2-3010 NERVE STIMULATOR
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EASYMED PERIPHERAL NERVE STIMULATOR-SUNSTIN
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Other Clearances by Neuro Technology
| K Number | Device Name | ||
|---|---|---|---|
| K925014 | E-SP COMBINED EPI SPINAL MINISET | Apr 19, 1993 | Unknown |
| K901810 | MICRO-SP LUMBAR PUNCTURE (SPINAL) NEEDLE | May 30, 1991 | Substantially Equivalent |
| K901811 | ADD'L DATA E-SP MULTIPURPOSE EPIDURAL SPINALNEEDLE | May 28, 1991 | Substantially Equivalent |
| K822138 | NEUROSTIM II | Jul 30, 1982 | Substantially Equivalent |