FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ENTROPY EASYFIT SENSOR
K Number: K103129
·
Decision Jul 19, 2011
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
188
Applicant Total
168
Review Days
270
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Basic Information
- Device Name
- ENTROPY EASYFIT SENSOR
- K Number
- K103129
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.1400
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- GE Healthcare
- Date Received
- October 22, 2010
- Decision Date
- July 19, 2011
- Product Code
- GWQ
- 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 |
|---|---|---|---|
| GWQ | Full-Montage Standard Electroencephalograph | FDA class 2 | Neurology |
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