FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MODEL 1310 NEUROLINK NEUROMONITORING SYSTEM
K Number: K962157
·
Decision Nov 25, 1996
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
188
Applicant Total
22
Review Days
174
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Basic Information
- Device Name
- MODEL 1310 NEUROLINK NEUROMONITORING SYSTEM
- K Number
- K962157
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.1400
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Physiometrix, Inc.
- Date Received
- June 4, 1996
- Decision Date
- November 25, 1996
- 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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| K970942 | MODEL 1320, NEUROLINK II NEUROMONITORING SYSTEM | Jun 2, 1997 | Substantially Equivalent |
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