FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇦 Canada
PROTEKTOR 32
K Number: K093304
·
Decision Aug 11, 2010
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
138
Applicant Total
12
Review Days
294
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Basic Information
- Device Name
- PROTEKTOR 32
- K Number
- K093304
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.1870
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Natus Medical, Inc.
- Date Received
- October 21, 2009
- Decision Date
- August 11, 2010
- Product Code
- GWF
- 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 |
|---|---|---|---|
| GWF | Stimulator, Electrical, Evoked Response | FDA class 2 | Neurology |
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