FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PRESSON ELECTRODE
K Number: K103103
·
Decision Dec 8, 2011
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
52
Applicant Total
4
Review Days
414
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Basic Information
- Device Name
- PRESSON ELECTRODE
- K Number
- K103103
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.1350
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Persyst Development Corp.
- Date Received
- October 20, 2010
- Decision Date
- December 8, 2011
- Product Code
- GXZ
- 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 |
|---|---|---|---|
| GXZ | Electrode, Needle | FDA class 2 | Neurology |
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